{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,7]],"date-time":"2026-11-07T11:29:17Z","timestamp":1794050957728,"version":"4.8.0"},"reference-count":103,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2021,8,20]],"date-time":"2021-08-20T00:00:00Z","timestamp":1629417600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2021,8,20]],"date-time":"2021-08-20T00:00:00Z","timestamp":1629417600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Mol Divers"],"published-print":{"date-parts":[[2022,6]]},"DOI":"10.1007\/s11030-021-10295-3","type":"journal-article","created":{"date-parts":[[2021,8,20]],"date-time":"2021-08-20T16:04:24Z","timestamp":1629475464000},"page":"1837-1873","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":81,"title":["Recent trends in the chemistry of Sandmeyer reaction: a review"],"prefix":"10.1007","volume":"26","author":[{"given":"Rabia","family":"Akhtar","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2127-8848","authenticated-orcid":false,"given":"Ameer Fawad","family":"Zahoor","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nasir","family":"Rasool","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matloob","family":"Ahmad","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kulsoom Ghulam","family":"Ali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2021,8,20]]},"reference":[{"key":"10295_CR1","doi-asserted-by":"publisher","first-page":"123","DOI":"10.1002\/jlac.18581060114","volume":"106","author":"P Griefs","year":"1858","unstructured":"P Griefs 1858 Vorl\u00e4ufige Notiz \u00fcber die Einwirkung von salpetriger S\u00e4ure auf Amidinitro-und Aminitrophenyls\u00e4ure Justus Liebigs Ann Chem 106 123 125 https:\/\/doi.org\/10.1002\/jlac.18581060114","journal-title":"Justus Liebigs Ann Chem"},{"key":"10295_CR2","doi-asserted-by":"publisher","first-page":"2163","DOI":"10.1002\/app.36394","volume":"125","author":"MAK Zarchi","year":"2012","unstructured":"MAK Zarchi N Ebrahimi 2012 Diazotization-cyanation of aromatic amines with crosslinked poly(4-vinylpyridine)-supported cyanide ions J Appl Polym Sci 125 2163 2169 https:\/\/doi.org\/10.1002\/app.36394","journal-title":"J Appl Polym Sci"},{"key":"10295_CR3","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1002\/prac.19391520705","volume":"152","author":"H Meerwein","year":"1939","unstructured":"H Meerwein E B\u00fcchner K Emster van 1939 \u00dcber die Einwirkung aromatischer Diazoverbindungen auf \u03b1, \u03b2-unges\u00e4ttigte Carbonylverbindungen J Prakt Chem 152 237 266 https:\/\/doi.org\/10.1002\/prac.19391520705","journal-title":"J Prakt Chem"},{"key":"10295_CR4","doi-asserted-by":"publisher","first-page":"725","DOI":"10.1002\/anie.201307051","volume":"53","author":"D Prasad-Hari","year":"2014","unstructured":"D Prasad-Hari T Hering B K\u00f6nig 2014 The photoredox-catalyzed Meerwein addition reaction: Intermolecular amino-arylation of alkenes Angew Chem Int Ed 53 725 728 https:\/\/doi.org\/10.1002\/anie.201307051","journal-title":"Angew Chem Int Ed"},{"key":"10295_CR5","doi-asserted-by":"publisher","first-page":"1186","DOI":"10.1002\/cber.19270600539","volume":"60","author":"G Balz","year":"1927","unstructured":"G Balz G Schiemann 1927 \u00dcber aromatische Fluorverbindungen, I.: Ein neues Verfahren zu ihrer Darstellung Ber Dtsch Chem Ges 60 1186 1190 https:\/\/doi.org\/10.1002\/cber.19270600539","journal-title":"Ber Dtsch Chem Ges"},{"key":"10295_CR6","doi-asserted-by":"publisher","first-page":"993","DOI":"10.1021\/op500100b","volume":"18","author":"S Abele","year":"2014","unstructured":"S Abele G Schmidt MJ Fleming H Steiner 2014 A One-pot diazotation-fluorodediazoniation reaction and fluorine gas for the production of fluoronaphthyridines Org Process Res Dev 18 993 1001 https:\/\/doi.org\/10.1021\/op500100b","journal-title":"Org Process Res Dev"},{"key":"10295_CR7","doi-asserted-by":"publisher","first-page":"4622","DOI":"10.1021\/cr0509861","volume":"106","author":"A Roglans","year":"2006","unstructured":"A Roglans A Pla-Quintana M Moreno-Ma\u00f1as 2006 Diazonium salts as substrates in palladium-catalyzed cross-coupling reactions Chem Rev 106 4622 4643 https:\/\/doi.org\/10.1021\/cr0509861","journal-title":"Chem Rev"},{"key":"10295_CR8","doi-asserted-by":"publisher","first-page":"1630","DOI":"10.1002\/ejoc.201301538","volume":"2014","author":"T Okazaki","year":"2014","unstructured":"T Okazaki KK Laali SD Bunge SK Adas 2014 4-(Pentafluorosulfanyl)benzenediazonium tetrafluoroborate: a versatile launch pad for the synthesis of aromatic SF5 compounds via cross Coupling, azo coupling, homocoupling, dediazoniation, and click chemistry Eur J Org Chem 2014 1630 1644 https:\/\/doi.org\/10.1002\/ejoc.201301538","journal-title":"Eur J Org Chem"},{"key":"10295_CR9","doi-asserted-by":"publisher","first-page":"6965","DOI":"10.1039\/C4OB01286K","volume":"12","author":"L He","year":"2014","unstructured":"L He G Qiu Y Gao J Wu 2014 Removal of amino groups from anilines through diazonium salt-based reactions Org Biomol Chem 12 6965 6971 https:\/\/doi.org\/10.1039\/C4OB01286K","journal-title":"Org Biomol Chem"},{"key":"10295_CR10","doi-asserted-by":"publisher","first-page":"648","DOI":"10.1021\/ol1028892","volume":"13","author":"PY Yeung","year":"2011","unstructured":"PY Yeung CM So CP Lau FY Kwong 2011 A mild and efficient palladium-catalyzed cyanation of aryl chlorides with K4[Fe(CN)6] Org Lett 13 648 651 https:\/\/doi.org\/10.1021\/ol1028892","journal-title":"Org Lett"},{"key":"10295_CR11","doi-asserted-by":"publisher","first-page":"8603","DOI":"10.1039\/C4OB01736F","volume":"12","author":"J Han","year":"2014","unstructured":"J Han C Pan X Jia C Zhu 2014 Rhodium-catalyzed ortho-cyanation of symmetrical azobenzenes with N-cyano-N-phenyl-p-toluenesulfonamide Org Biomol Chem 12 8603 8606 https:\/\/doi.org\/10.1039\/C4OB01736F","journal-title":"Org Biomol Chem"},{"key":"10295_CR12","doi-asserted-by":"publisher","first-page":"1838","DOI":"10.1039\/B404699D","volume":"2","author":"P Hanson","year":"2004","unstructured":"P Hanson SC Rowell PH Walton AW Timms 2004 Promotion of Sandmeyer hydroxylation (homolytic hydroxydediazoniation) and hydrodediazoniation by chelation of the copper catalyst: Bidentate ligands Org Biomol Chem 2 1838 1855 https:\/\/doi.org\/10.1039\/B404699D","journal-title":"Org Biomol Chem"},{"key":"10295_CR13","doi-asserted-by":"publisher","first-page":"12078","DOI":"10.1002\/ange.201305902","volume":"125","author":"F Xie","year":"2013","unstructured":"F Xie Z Qi X Li 2013 Rhodium(III)-catalyzed azidation and nitration of arenes by CH activation Angew Chem 125 12078 12082 https:\/\/doi.org\/10.1002\/ange.201305902","journal-title":"Angew Chem"},{"key":"10295_CR14","doi-asserted-by":"publisher","first-page":"423","DOI":"10.1002\/rcm.4869","volume":"25","author":"BV Silva","year":"2011","unstructured":"BV Silva FA Violante AC Pinto LS Santos 2011 The mechanism of Sandmeyer\u2019s cyclization reaction by electrospray ionization mass spectrometry Rapid Commun Mass Spectrom 25 423 428 https:\/\/doi.org\/10.1002\/rcm.4869","journal-title":"Rapid Commun Mass Spectrom"},{"key":"10295_CR15","doi-asserted-by":"publisher","first-page":"167","DOI":"10.1080\/00397911.2018.1514636","volume":"49","author":"R Akhtar","year":"2019","unstructured":"R Akhtar AF Zahoor B Parveen M Suleman 2019 Development of environmental friendly synthetic strategies for Sonogashira cross coupling reaction: an update Synthetic Commun 49 167 192 https:\/\/doi.org\/10.1080\/00397911.2018.1514636","journal-title":"Synthetic Commun"},{"key":"10295_CR16","doi-asserted-by":"publisher","first-page":"3337","DOI":"10.1080\/00397911.2020.1802757","volume":"50","author":"R Akhtar","year":"2020","unstructured":"R Akhtar AF Zahoor 2020 Transition metal catalyzed Glaser and Glaser-Hay coupling reactions: scope, classical\/green methodologies and synthetic applications Syn Commun 50 3337 3368 https:\/\/doi.org\/10.1080\/00397911.2020.1802757","journal-title":"Syn Commun"},{"key":"10295_CR17","doi-asserted-by":"publisher","first-page":"821","DOI":"10.1007\/s11030-019-09988-7","volume":"24","author":"M Yousaf","year":"2020","unstructured":"M Yousaf AF Zahoor R Akhtar M Ahmad S Naheed 2020 Development of green methodologies for Heck, Chan-Lam, Stille and Suzuki cross-coupling reactions Mol Divers 24 821 839 https:\/\/doi.org\/10.1007\/s11030-019-09988-7","journal-title":"Mol Divers"},{"key":"10295_CR18","doi-asserted-by":"publisher","DOI":"10.1007\/s11030-021-10195-6","author":"S Tabassum","year":"2021","unstructured":"S Tabassum AF Zahoor S Ahmad R Noreen SG Khan H Ahmad 2021 Cross-coupling reactions towards the synthesis of natural products Mol Divers In press https:\/\/doi.org\/10.1007\/s11030-021-10195-6","journal-title":"Mol Divers In press"},{"key":"10295_CR19","doi-asserted-by":"publisher","first-page":"215","DOI":"10.1007\/s11030-018-9870-z","volume":"23","author":"I Munir","year":"2019","unstructured":"I Munir AF Zahoor N Rasool SAR Naqvi KM Zia R Ahmad 2019 Synthetic applications and methodology development of Chan-Lam coupling: a review Mol Divers 23 215 259 https:\/\/doi.org\/10.1007\/s11030-018-9870-z","journal-title":"Mol Divers"},{"key":"10295_CR20","doi-asserted-by":"publisher","first-page":"1633","DOI":"10.1002\/cber.18840170219","volume":"17","author":"T Sandmeyer","year":"1884","unstructured":"T Sandmeyer 1884 Ueber die Ersetzung der Amidgruppe durch Chlor in den aromatischen Substanzen Ber Dtsch Chem Ges 17 1633 1635 https:\/\/doi.org\/10.1002\/cber.18840170219","journal-title":"Ber Dtsch Chem Ges"},{"key":"10295_CR21","doi-asserted-by":"publisher","first-page":"2650","DOI":"10.1002\/cber.188401702202","volume":"17","author":"T Sandmeyer","year":"1884","unstructured":"T Sandmeyer 1884 Ueber die Ersetzung der Amidgruppe durch Chlor, Brom und Cyan in den aromatischen Substanzen Ber Dtsch Chem Ges 17 2650 2653 https:\/\/doi.org\/10.1002\/cber.188401702202","journal-title":"Ber Dtsch Chem Ges"},{"key":"10295_CR22","doi-asserted-by":"publisher","first-page":"2426","DOI":"10.1021\/jo00434a017","volume":"42","author":"MP Doyle","year":"1977","unstructured":"MP Doyle B Siegfried JF Dellaria 1977 Alkyl nitrite-metal halide deamination reactions. 2. Substitutive deamination of arylamines by alkyl nitrites and copper(II) halides. A direct and remarkably efficient conversion of arylamines to aryl halides J Org Chem 42 2426 2431 https:\/\/doi.org\/10.1021\/jo00434a017","journal-title":"J Org Chem"},{"key":"10295_CR23","doi-asserted-by":"publisher","first-page":"3494","DOI":"10.1021\/jo00442a009","volume":"42","author":"MP Doyle","year":"1977","unstructured":"MP Doyle JF Dellaria B Siegfried SW Bishop 1977 Reductive deamination of arylamines by alkyl nitrites in N, N-dimethylformamide. A direct conversion of arylamines to aromatic hydrocarbons J Org Chem 42 3494 3498 https:\/\/doi.org\/10.1021\/jo00442a009","journal-title":"J Org Chem"},{"key":"10295_CR24","doi-asserted-by":"publisher","first-page":"159","DOI":"10.1246\/cl.1977.159","volume":"6","author":"K Kikukawa","year":"1977","unstructured":"K Kikukawa T Matsuda 1977 Reaction of diazonium salts with transition metals. I. Arylation of olefins with arenediazonium salts catalyzed by zero valent palladium Chem Lett 6 159 162 https:\/\/doi.org\/10.1246\/cl.1977.159","journal-title":"Chem Lett"},{"key":"10295_CR25","doi-asserted-by":"publisher","first-page":"2609","DOI":"10.1246\/bcsj.52.2609","volume":"52","author":"K Kikukawa","year":"1979","unstructured":"K Kikukawa K Nagira N Terao F Wada T Matsuda 1979 Reaction of diazonium salts with transition metals. II. Palladium catalyzed arylation of ethylene with arenediazonium salts Bull Chem Soc Jpn 52 2609 2610 https:\/\/doi.org\/10.1246\/bcsj.52.2609","journal-title":"Bull Chem Soc Jpn"},{"key":"10295_CR26","doi-asserted-by":"publisher","unstructured":"Waters WA (1942) Decomposition reactions of the aromatic diazo compounds. X. Mechanism of the Sandmeyer reaction. J Chem Soc 266\u2013270. https:\/\/doi.org\/10.1039\/JR9420000266","DOI":"10.1039\/JR9420000266"},{"key":"10295_CR27","doi-asserted-by":"publisher","first-page":"2942","DOI":"10.1021\/ja01568a066","volume":"79","author":"JK Kochi","year":"1957","unstructured":"JK Kochi 1957 The mechanism of the Sandmeyer and Meerwein reactions J Am Chem Soc 79 2942 2948 https:\/\/doi.org\/10.1021\/ja01568a066","journal-title":"J Am Chem Soc"},{"key":"10295_CR28","doi-asserted-by":"publisher","first-page":"5043","DOI":"10.1039\/C1CC10641D","volume":"47","author":"D Sucunza","year":"2011","unstructured":"D Sucunza A Samadi M Chioua DB Silva C Yunta L Infantes MC Carreiras E Sorianoa J Marco-Contelles 2011 A practical two-step synthesis of imidazo[1,2-a]pyridines from N-(prop-2-yn-1-yl)pyridin-2-amines Chem Commun 47 5043 5045 https:\/\/doi.org\/10.1039\/C1CC10641D","journal-title":"Chem Commun"},{"key":"10295_CR29","doi-asserted-by":"publisher","first-page":"4135","DOI":"10.1016\/j.tet.2008.01.003","volume":"64","author":"R Sott","year":"2008","unstructured":"R Sott C Hawner JE Johansen 2008 Synthesis of dioxin-like monofluorinated PCBs: For the use as internal standards for PCB analysis Tetrahedron 64 4135 4142 https:\/\/doi.org\/10.1016\/j.tet.2008.01.003","journal-title":"Tetrahedron"},{"key":"10295_CR30","doi-asserted-by":"publisher","first-page":"1150","DOI":"10.1055\/s-0033-1338433","volume":"24","author":"R Dumeunier","year":"2013","unstructured":"R Dumeunier C Lamberth S Trah 2013 Synthesis of tetrasubstituted pyrazoles through different cyclization Strategies; Isosteres of imidazole fungicides Synlett 24 1150 1154 https:\/\/doi.org\/10.1055\/s-0033-1338433","journal-title":"Synlett"},{"key":"10295_CR31","doi-asserted-by":"publisher","first-page":"3266","DOI":"10.1016\/j.bmcl.2007.04.021","volume":"17","author":"TV Hughes","year":"2007","unstructured":"TV Hughes SL Emanuel AK Beck SK Wetter PJ Connolly P Karnachi M Reuman J Seraj AR Fuentes-Pesquera RH Gruninger SA Middleton R Lin JM Davis DFC Moffat 2007 4-Aryl-5-cyano-2-aminopyrimidines as VEGF-R2 inhibitors: Synthesis and biological evaluation Bioorganic Med Chem Lett 17 3266 3270 https:\/\/doi.org\/10.1016\/j.bmcl.2007.04.021","journal-title":"Bioorganic Med Chem Lett"},{"key":"10295_CR32","doi-asserted-by":"publisher","first-page":"2507","DOI":"10.1080\/00397910802219148","volume":"38","author":"F Rancati","year":"2008","unstructured":"F Rancati SM Bromidge SD Sordo SL Rosa C Parini S Gagliardi 2008 Synthesis of 7-substituted-(2,3-dihydro-1,4-benzodioxin-5-yl)-piperazine Synth Commun 38 2507 2520 https:\/\/doi.org\/10.1080\/00397910802219148","journal-title":"Synth Commun"},{"key":"10295_CR33","doi-asserted-by":"publisher","first-page":"2655","DOI":"10.1016\/j.bmcl.2014.04.058","volume":"24","author":"C-H Park","year":"2014","unstructured":"C-H Park C Lee JS Yang B-Y Joe K Chun H Kim HY Kim JS Kang JI Lee M-H Kim G Han 2014 Discovery of thienopyrimidine-based FLT3 inhibitors from the structural modification of known IKK inhibitors Bioorganic Med Chem Lett 24 2655 2660 https:\/\/doi.org\/10.1016\/j.bmcl.2014.04.058","journal-title":"Bioorganic Med Chem Lett"},{"key":"10295_CR34","doi-asserted-by":"publisher","first-page":"176","DOI":"10.3390\/molecules26010176","volume":"26","author":"Y Ding","year":"2021","unstructured":"Y Ding L Zhao Y Fu L Hao Y Fu Y Yuan P Yu Y Teng 2021 Synthesis and antiproliferatory activities evaluation of multi-substituted isatin derivatives Molecules 26 176 189 https:\/\/doi.org\/10.3390\/molecules26010176","journal-title":"Molecules"},{"key":"10295_CR35","doi-asserted-by":"publisher","first-page":"6266","DOI":"10.1016\/j.bmcl.2007.09.013","volume":"17","author":"L Lee","year":"2007","unstructured":"L Lee KD Kreutter W Pan C Crysler J Spurlino MR Player B Tomczuk T Lu 2007 2-(2-Chloro-6-fluorophenyl)acetamides as potent thrombin inhibitors Bioorganic Med Chem Lett 17 6266 6269 https:\/\/doi.org\/10.1016\/j.bmcl.2007.09.013","journal-title":"Bioorganic Med Chem Lett"},{"key":"10295_CR36","doi-asserted-by":"publisher","first-page":"11382","DOI":"10.1039\/C1DT11327E","volume":"40","author":"TS Lobana","year":"2011","unstructured":"TS Lobana R Sultana RJ Butcher 2011 A Sandmeyer type reaction for bromination of 2-mercapto-1-methyl-imidazoline (N2C4H6S) into 2-bromo-1-methyl-imidazole (N2C4H5Br) in presence of copper(I) bromide Dalton Trans 40 11382 11384 https:\/\/doi.org\/10.1039\/C1DT11327E","journal-title":"Dalton Trans"},{"key":"10295_CR37","doi-asserted-by":"publisher","first-page":"316","DOI":"10.1021\/jo701937e","volume":"73","author":"A Hubbard","year":"2008","unstructured":"A Hubbard T Okazaki KK Laali 2008 Halo- and azidodediazoniation of arenediazonium tetrafluoroborates with trimethylsilyl halides and trimethylsilyl azide and Sandmeyer-type bromodediazoniation with Cu(I)Br in [BMIM][PF6] ionic liquid J Org Chem 73 316 319 https:\/\/doi.org\/10.1021\/jo701937e","journal-title":"J Org Chem"},{"key":"10295_CR38","doi-asserted-by":"publisher","first-page":"3906","DOI":"10.1021\/ol301655f","volume":"14","author":"MA Bobko","year":"2012","unstructured":"MA Bobko AC Kaura KA Evans D-S Su 2012 Novel synthesis of 5-amino-3-bromo- 1-(tert-butyl)-1H-pyrazole-4-carbonitrile: A versatile intermediate for the preparation of 5-amino-3-aryl-1-(tert-butyl)-1H-pyrazole-4-carboxamides Org Lett 14 3906 3908 https:\/\/doi.org\/10.1021\/ol301655f","journal-title":"Org Lett"},{"key":"10295_CR39","doi-asserted-by":"publisher","first-page":"2478","DOI":"10.3390\/12112478","volume":"12","author":"H \u00d6zkan","year":"2007","unstructured":"H \u00d6zkan A Di\u015fli Y Y\u0131ld\u0131r\u0131r L T\u00fcrker 2007 A novel synthesis of bromobenzenes using molecular bromine Molecules 12 2478 2483 https:\/\/doi.org\/10.3390\/12112478","journal-title":"Molecules"},{"key":"10295_CR40","doi-asserted-by":"publisher","first-page":"228","DOI":"10.1021\/acs.oprd.9b00495","volume":"24","author":"G Sch\u00e4fer","year":"2020","unstructured":"G Sch\u00e4fer T Fleischer M Ahmetovic S Abele 2020 Development of a scalable route for a key thiadiazole building block via sequential Sandmeyer bromination and room-temperature Suzuki-Miyaura coupling Org Process Res Dev 24 228 234 https:\/\/doi.org\/10.1021\/acs.oprd.9b00495","journal-title":"Org Process Res Dev"},{"key":"10295_CR41","doi-asserted-by":"publisher","first-page":"1681","DOI":"10.1016\/j.tetlet.2017.03.029","volume":"58","author":"R Striela","year":"2017","unstructured":"R Striela G Urbelis J S\u016bd\u017eius S Ston\u010dius R Sadzevi\u010dien\u0117 L Labanauskas 2017 Synthesis of bromocyclopropylpyridines via the Sandmeyer reaction Tetrahedron Lett 58 1681 1683 https:\/\/doi.org\/10.1016\/j.tetlet.2017.03.029","journal-title":"Tetrahedron Lett"},{"key":"10295_CR42","doi-asserted-by":"publisher","first-page":"2534","DOI":"10.1055\/s-2007-983784","volume":"16","author":"IP Beletskaya","year":"2007","unstructured":"IP Beletskaya AS Sigeev AS Peregudov PV Petrovskii 2007 Catalytic Sandmeyer bromination Synthesis 16 2534 2538 https:\/\/doi.org\/10.1055\/s-2007-983784","journal-title":"Synthesis"},{"key":"10295_CR43","doi-asserted-by":"publisher","first-page":"2578","DOI":"10.1021\/jo802799c","volume":"74","author":"FG Sim\u00e9on","year":"2009","unstructured":"FG Sim\u00e9on MT Wendahl VW Pike 2009 Efficient and regioselective halogenations of 2-amino-1,3-thiazoles with copper salts J Org Chem 74 2578 2580 https:\/\/doi.org\/10.1021\/jo802799c","journal-title":"J Org Chem"},{"key":"10295_CR44","doi-asserted-by":"publisher","first-page":"4570","DOI":"10.1016\/j.bmcl.2009.06.098","volume":"19","author":"WW Mao","year":"2009","unstructured":"WW Mao TT Wang HP Zeng ZY Wang JP Chen JG Shen 2009 Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant anti-proliferative activity against breast cancer cell lines Bioorg Med Chem Lett 19 4570 4573 https:\/\/doi.org\/10.1016\/j.bmcl.2009.06.098","journal-title":"Bioorg Med Chem Lett"},{"key":"10295_CR45","doi-asserted-by":"publisher","first-page":"3185","DOI":"10.1021\/ol071320r","volume":"9","author":"H-Y Kim","year":"2007","unstructured":"H-Y Kim W-J Lee H-M Kang C-G Cho 2007 Benzidine rearrangement reactions of polyether tethered cyclic N, N\u2032-diaryl hydrazides Org Lett 9 3185 3186 https:\/\/doi.org\/10.1021\/ol071320r","journal-title":"Org Lett"},{"key":"10295_CR46","doi-asserted-by":"publisher","first-page":"521","DOI":"10.1039\/C4TC02339K","volume":"3","author":"M Gon","year":"2015","unstructured":"M Gon Y Morisaki Y Chujo 2015 Optically active cyclic compounds based on planar chiral [2.2]paracyclophane: extension of the conjugated systems and chiroptical properties J Mater Chem C 3 521 529 https:\/\/doi.org\/10.1039\/C4TC02339K","journal-title":"J Mater Chem C"},{"key":"10295_CR47","doi-asserted-by":"publisher","first-page":"8731","DOI":"10.1039\/C8SC03346C","volume":"9","author":"Q Liu","year":"2018","unstructured":"Q Liu B Sun Z Liu Y Kao B-W Dong S-D Jiang F Li G Liu Y Yang F Mo 2018 A general electrochemical strategy for Sandmeyer reaction Chem Sci 9 8731 8737 https:\/\/doi.org\/10.1039\/C8SC03346C","journal-title":"Chem Sci"},{"key":"10295_CR48","doi-asserted-by":"publisher","first-page":"6589","DOI":"10.1016\/S0040-4039(01)01302-8","volume":"42","author":"PG Tsoungas","year":"2001","unstructured":"PG Tsoungas M Searcey 2001 A convenient access to benzo-substituted phthalazines as potential precursors to DNA intercalators Tetrahedron Lett 42 6589 6592 https:\/\/doi.org\/10.1016\/S0040-4039(01)01302-8","journal-title":"Tetrahedron Lett"},{"key":"10295_CR49","doi-asserted-by":"publisher","first-page":"78","DOI":"10.3998\/ark.5550190.0007.507","volume":"2006","author":"R Bucht\u00edk","year":"2006","unstructured":"R Bucht\u00edk J Slouka J Hlav\u00e1\u010d 2006 Polycyclic heterocycles with acidic N-H group VII1 Synthesis of some polynuclear heterocyclic compounds derived from 5-phenyl-6-azauracil ARKIVOC 2006 78 85 https:\/\/doi.org\/10.3998\/ark.5550190.0007.507","journal-title":"ARKIVOC"},{"key":"10295_CR50","doi-asserted-by":"publisher","first-page":"1761","DOI":"10.1002\/cjoc.201700311","volume":"35","author":"J Hong","year":"2017","unstructured":"J Hong G Wang L Huo C Zheng 2017 Copper-promoted conversion of aromatic amines into trifluoromethylated arenes: one-pot Sandmeyer trifluoromethylation Chin J Chem 35 1761 1767 https:\/\/doi.org\/10.1002\/cjoc.201700311","journal-title":"Chin J Chem"},{"key":"10295_CR51","doi-asserted-by":"publisher","first-page":"1312","DOI":"10.1039\/C3SC53076K","volume":"5","author":"G Danoun","year":"2014","unstructured":"G Danoun B Bayarmagnai MF Gruenberg LJ Goossen 2014 Sandmeyer trifluoromethylthiolation of arenediazonium salts with sodium thiocyanate and Ruppert-Prakash reagent Chem Sci 5 1312 1316 https:\/\/doi.org\/10.1039\/C3SC53076K","journal-title":"Chem Sci"},{"key":"10295_CR52","doi-asserted-by":"publisher","first-page":"2283","DOI":"10.1055\/s-0034-1378549","volume":"46","author":"G Danoun","year":"2014","unstructured":"G Danoun B Bayarmagnai MF Gruenberg C Matheis E Risto LJ Goo\u00dfen 2014 Sandmeyer trifluoromethylation Synthesis 46 2283 2286 https:\/\/doi.org\/10.1055\/s-0034-1378549","journal-title":"Synthesis"},{"key":"10295_CR53","doi-asserted-by":"publisher","first-page":"7972","DOI":"10.1002\/anie.201304276","volume":"52","author":"G Danoun","year":"2013","unstructured":"G Danoun B Bayarmagnai MF Gruenberg LJ Goo\u00dfen 2013 Sandmeyer trifluoromethylation of arenediazonium tetrafluoroborates Angew Chem Int Ed 52 7972 7975 https:\/\/doi.org\/10.1002\/anie.201304276","journal-title":"Angew Chem Int Ed"},{"key":"10295_CR54","doi-asserted-by":"publisher","first-page":"2343","DOI":"10.1002\/adsc.201400340","volume":"356","author":"B Bayarmagnai","year":"2014","unstructured":"B Bayarmagnai C Matheis E Risto LJ Goossen 2014 One-pot Sandmeyer trifluoromethylation and trifluoromethylthiolation Adv Synth Catal 356 2343 2348 https:\/\/doi.org\/10.1002\/adsc.201400340","journal-title":"Adv Synth Catal"},{"key":"10295_CR55","doi-asserted-by":"publisher","first-page":"8436","DOI":"10.1021\/ja404217t","volume":"135","author":"J-J Dai","year":"2013","unstructured":"J-J Dai C Fang B Xiao J Yi J Xu ZJ Liu X Lu L Liu Y Fu 2013 Copper-promoted Sandmeyer trifluoromethylation reaction J Am Chem Soc 135 8436 8439 https:\/\/doi.org\/10.1021\/ja404217t","journal-title":"J Am Chem Soc"},{"key":"10295_CR56","doi-asserted-by":"publisher","first-page":"5984","DOI":"10.1021\/ol5030037","volume":"16","author":"C Matheis","year":"2014","unstructured":"C Matheis K Jouvin LJ Goossen 2014 Sandmeyer difluoromethylation of (hetero)arenediazonium salts Org Lett 16 5984 5987 https:\/\/doi.org\/10.1021\/ol5030037","journal-title":"Org Lett"},{"key":"10295_CR57","doi-asserted-by":"publisher","first-page":"2143","DOI":"10.1055\/s-0033-1338659","volume":"46","author":"X Wang","year":"2014","unstructured":"X Wang Y Xu Y Zhou Y Zhang J Wang 2014 Conversion of aromatic amino into trifluoromethyl groups through a Sandmeyer-type transformation Synthesis 46 2143 2148 https:\/\/doi.org\/10.1055\/s-0033-1338659","journal-title":"Synthesis"},{"key":"10295_CR58","doi-asserted-by":"publisher","first-page":"7758","DOI":"10.1002\/ange.201502113","volume":"127","author":"J Wu","year":"2015","unstructured":"J Wu Y Gu X Leng Q Shen 2015 Copper-promoted Sandmeyer difluoromethylthiolation of aryl and heteroaryl diazonium salts Angew Chem 127 7758 7762 https:\/\/doi.org\/10.1002\/ange.201502113","journal-title":"Angew Chem"},{"key":"10295_CR59","doi-asserted-by":"publisher","first-page":"1131","DOI":"10.1002\/cjoc.201900268","volume":"37","author":"B Xing","year":"2019","unstructured":"B Xing L Li C Ni J Hu 2019 Pentafluoroethylation of arenediazonium tetrafluoroborates using on-site generated tetrafluoroethylene Chin J Chem 37 1131 1136 https:\/\/doi.org\/10.1002\/cjoc.201900268","journal-title":"Chin J Chem"},{"key":"10295_CR60","doi-asserted-by":"publisher","first-page":"3716","DOI":"10.1002\/slct.201700789","volume":"2","author":"J Hong","year":"2017","unstructured":"J Hong L Huo Y Yang G Wang C Zheng 2017 Copper-promoted one-pot trifluoromethylation of aromatic amines with Togni\u2019s reagent ChemistrySelect 2 3716 3720 https:\/\/doi.org\/10.1002\/slct.201700789","journal-title":"ChemistrySelect"},{"key":"10295_CR61","doi-asserted-by":"publisher","first-page":"6303","DOI":"10.1002\/ejoc.201402820","volume":"2014","author":"D-F Jiang","year":"2014","unstructured":"D-F Jiang C Liu Y Guo JC Xiao QY Chen 2014 A general, regiospecific synthetic route to perfluoroalkylated arenes via arenediazonium salts with RFCu(CH3CN) complexes Eur J Org Chem 2014 6303 6309 https:\/\/doi.org\/10.1002\/ejoc.201402820","journal-title":"Eur J Org Chem"},{"key":"10295_CR62","doi-asserted-by":"publisher","first-page":"10237","DOI":"10.1039\/C4CC04930F","volume":"50","author":"A Lishchynskyi","year":"2014","unstructured":"A Lishchynskyi G Berthon VV Grushin 2014 Trifluoromethylation of arenediazonium salts with fluoroform-derived CuCF3 in aqueous media Chem Commun 50 10237 10240 https:\/\/doi.org\/10.1039\/C4CC04930F","journal-title":"Chem Commun"},{"key":"10295_CR63","doi-asserted-by":"publisher","first-page":"1062","DOI":"10.1002\/ajoc.201402084","volume":"3","author":"W-B Xu","year":"2014","unstructured":"W-B Xu Q-H Xu Z-F Zhang J-Z Li 2014 Copper(I)-oxide-mediated cyanation of arenediazonium tetrafluoroborates with trimethylsilyl cyanide: A method for synthesizing aromatic nitriles Asian J Org Chem 3 1062 1065 https:\/\/doi.org\/10.1002\/ajoc.201402084","journal-title":"Asian J Org Chem"},{"key":"10295_CR64","doi-asserted-by":"publisher","first-page":"231","DOI":"10.1039\/C4QO00301B","volume":"2","author":"W Xu","year":"2015","unstructured":"W Xu Q Xu J Li 2015 Sandmeyer cyanation of arenediazonium tetrafluoroborate using acetonitrile as cyanide source Org Chem Front 2 231 235 https:\/\/doi.org\/10.1039\/C4QO00301B","journal-title":"Org Chem Front"},{"key":"10295_CR65","doi-asserted-by":"publisher","first-page":"1437","DOI":"10.1039\/C5OB02321A","volume":"14","author":"M Barbero","year":"2016","unstructured":"M Barbero S Cadamuro S Dughera 2016 Copper-free Sandmeyer cyanation of arenediazonium o-benzenedisulfonimide Org Biomol Chem 14 1437 1441 https:\/\/doi.org\/10.1039\/C5OB02321A","journal-title":"Org Biomol Chem"},{"key":"10295_CR66","doi-asserted-by":"publisher","first-page":"2725","DOI":"10.1055\/s-0030-1258149","volume":"16","author":"D Da Silva","year":"2010","unstructured":"D Silva Da A Samadi M Chioua MDC Carreiras J Marco-Contelles 2010 The Sandmeyer reaction on some selected heterocyclic ring systems: Synthesis of useful 2-chloroheterocyclic-3-carbonitrile intermediates Synthesis 16 2725 2730 https:\/\/doi.org\/10.1055\/s-0030-1258149","journal-title":"Synthesis"},{"key":"10295_CR67","doi-asserted-by":"publisher","first-page":"364","DOI":"10.1016\/j.ejmech.2010.10.022","volume":"46","author":"H Xu","year":"2011","unstructured":"H Xu L-L Fan 2011 Antifungal agents. Part 4: Synthesis and antifungal activities of novel indole[1,2-c]-1,2,4-benzotriazine derivatives against phytopathogenic fungi in vitro Eur J Med Chem 46 364 369 https:\/\/doi.org\/10.1016\/j.ejmech.2010.10.022","journal-title":"Eur J Med Chem"},{"key":"10295_CR68","doi-asserted-by":"publisher","first-page":"3810","DOI":"10.1016\/j.jorganchem.2004.07.019","volume":"689","author":"IP Beletskaya","year":"2004","unstructured":"IP Beletskaya AS Sigeev AS Peregudov PV Petrovskii 2004 Catalytic Sandmeyer cyanation as a synthetic pathway to aryl nitriles J Organomet Chem 689 3810 3812 https:\/\/doi.org\/10.1016\/j.jorganchem.2004.07.019","journal-title":"J Organomet Chem"},{"key":"10295_CR69","doi-asserted-by":"publisher","first-page":"1107","DOI":"10.1002\/cjoc.202000175","volume":"38","author":"Q Lin","year":"2020","unstructured":"Q Lin Z Ma C Zheng X-J Hu Y Guo Q-Y Chen C Liu 2020 Arenesulfonyl fluoride synthesis via copper-free Sandmeyer-type fluorosulfonylation of arenediazonium salts Chin J Chem 38 1107 1110 https:\/\/doi.org\/10.1002\/cjoc.202000175","journal-title":"Chin J Chem"},{"key":"10295_CR70","doi-asserted-by":"publisher","first-page":"0847","DOI":"10.1055\/S-0033-1340736","volume":"25","author":"X Yang","year":"2014","unstructured":"X Yang L Shi H Fu 2014 Copper-mediated cascade synthesis of diaryl sulfones via the Sandmeyer reaction Synlett 25 0847 0852 https:\/\/doi.org\/10.1055\/S-0033-1340736","journal-title":"Synlett"},{"key":"10295_CR71","doi-asserted-by":"publisher","first-page":"5845","DOI":"10.1002\/ange.201500899","volume":"127","author":"B Bayarmagnai","year":"2015","unstructured":"B Bayarmagnai C Matheis K Jouvin LJ Goossen 2015 Synthesis of difluoromethyl thioethers from difluoromethyl trimethylsilane and organothiocyanates generated in situ Angew Chem 127 5845 5848 https:\/\/doi.org\/10.1002\/ange.201500899","journal-title":"Angew Chem"},{"key":"10295_CR72","doi-asserted-by":"publisher","first-page":"79","DOI":"10.1002\/chem.201503524","volume":"22","author":"C Matheis","year":"2016","unstructured":"C Matheis V Wagner LJ Goossen 2016 Sandmeyer-type trifluoromethylthiolation and trifluoromethylselenolation of (hetero)aromatic amines catalyzed by copper Chem Eur J 22 79 82 https:\/\/doi.org\/10.1002\/chem.201503524","journal-title":"Chem Eur J"},{"key":"10295_CR73","doi-asserted-by":"publisher","first-page":"949","DOI":"10.1039\/C6QO00194G","volume":"3","author":"C Matheis","year":"2016","unstructured":"C Matheis B Bayarmagnai K Jouvin LJ Goossen 2016 Convenient synthesis of pentafluoroethyl thioethers via catalytic Sandmeyer reaction with a stable fluoroalkylthiolation reagent Org Chem Front 3 949 952 https:\/\/doi.org\/10.1039\/C6QO00194G","journal-title":"Org Chem Front"},{"key":"10295_CR74","doi-asserted-by":"publisher","first-page":"7658","DOI":"10.1021\/acs.joc.5b01295","volume":"80","author":"K Zhang","year":"2015","unstructured":"K Zhang X-H Xu F-L Qing 2015 Copper-promoted trifluoromethanesulfonylation and trifluoromethylation of arenediazonium tetrafluoroborates with NaSO2CF3 J Org Chem 80 7658 7665 https:\/\/doi.org\/10.1021\/acs.joc.5b01295","journal-title":"J Org Chem"},{"key":"10295_CR75","doi-asserted-by":"publisher","first-page":"1913","DOI":"10.1002\/adsc.201701549","volume":"360","author":"S Kovacs","year":"2018","unstructured":"S Kovacs B Bayarmagnai A Aillerie LJ Goo\u00dfen 2018 Practical reagents and methods for nucleophilic and electrophilic phosphorothiolations Adv Synth Catal 360 1913 1918 https:\/\/doi.org\/10.1002\/adsc.201701549","journal-title":"Adv Synth Catal"},{"key":"10295_CR76","doi-asserted-by":"publisher","first-page":"650","DOI":"10.1002\/ajoc.201800461","volume":"8","author":"Y Ou","year":"2019","unstructured":"Y Ou LJ Goossen 2019 Copper-mediated synthesis of (diethylphosphono)difluoromethyl thioethers from diazonium salts, NaSCN, and TMS-CF2PO(OEt)2 Asian J Org Chem 8 650 653 https:\/\/doi.org\/10.1002\/ajoc.201800461","journal-title":"Asian J Org Chem"},{"key":"10295_CR77","doi-asserted-by":"publisher","DOI":"10.1016\/j.jfluchem.2020.109653","volume":"240","author":"S Liu","year":"2020","unstructured":"S Liu Y Huang X-H Xu F-L Qing 2020 Fluorosulfonylation of arenediazonium tetrafluoroborates with Na2S2O5 and N-fluorobenzenesulfonimide J Fluor Chem 240 109653 https:\/\/doi.org\/10.1016\/j.jfluchem.2020.109653","journal-title":"J Fluor Chem"},{"key":"10295_CR78","doi-asserted-by":"publisher","first-page":"3072","DOI":"10.1021\/acs.orglett.0c00823","volume":"22","author":"T Zhong","year":"2020","unstructured":"T Zhong M-K Pang Z-D Chen B Zhang J Weng G Lu 2020 Copper-free Sandmeyer-type reaction for the synthesis of sulfonyl fluorides Org Lett 22 3072 3078 https:\/\/doi.org\/10.1021\/acs.orglett.0c00823","journal-title":"Org Lett"},{"key":"10295_CR79","doi-asserted-by":"publisher","first-page":"261","DOI":"10.1016\/j.mencom.2018.05.010","volume":"28","author":"IG Tarkhanova","year":"2018","unstructured":"IG Tarkhanova MG Gantman AS Sigeev KI Maslakov VM Zelikman IP Beletskaya 2018 Highly efficient Sandmeyer reaction on immobilized CuI\/CuII-based catalysts Mendeleev Commun 28 261 263 https:\/\/doi.org\/10.1016\/j.mencom.2018.05.010","journal-title":"Mendeleev Commun"},{"key":"10295_CR80","doi-asserted-by":"publisher","first-page":"11795","DOI":"10.1002\/ange.201304579","volume":"125","author":"D Qiu","year":"2013","unstructured":"D Qiu H Meng L Jin S Wang S Tang X Wang F Mo Y Zhang J Wang 2013 Synthesis of aryl trimethylstannanes from aryl amines: a Sandmeyer-type stannylation reaction Angew Chem 125 11795 11798 https:\/\/doi.org\/10.1002\/ange.201304579","journal-title":"Angew Chem"},{"key":"10295_CR81","doi-asserted-by":"publisher","first-page":"1979","DOI":"10.1021\/jo402618r","volume":"79","author":"D Qiu","year":"2014","unstructured":"D Qiu S Wang S Tang H Meng L Jin F Mo Y Zhang J Wang 2014 Synthesis of trimethylstannyl arylboronate compounds by Sandmeyer-type transformations and their applications in chemoselective cross-coupling reactions J Org Chem 79 1979 1988 https:\/\/doi.org\/10.1021\/jo402618r","journal-title":"J Org Chem"},{"key":"10295_CR82","doi-asserted-by":"publisher","first-page":"11603","DOI":"10.1021\/acs.joc.6b01820","volume":"81","author":"S Wang","year":"2016","unstructured":"S Wang D Qiu F Mo Y Zhang J Wang 2016 Metal-free aromatic carbon-phosphorus bond formation via a Sandmeyer-type reaction J Org Chem 81 11603 11611 https:\/\/doi.org\/10.1021\/acs.joc.6b01820","journal-title":"J Org Chem"},{"key":"10295_CR83","doi-asserted-by":"publisher","first-page":"2620","DOI":"10.1002\/chem.201504601","volume":"22","author":"P Nikolaienko","year":"2016","unstructured":"P Nikolaienko M Rueping 2016 Trifluoromethylselenolation of aryldiazonium salts: a mild and convenient copper-catalyzed procedure for the introduction of the SeCF3 group Chem Eur J 22 2620 2623 https:\/\/doi.org\/10.1002\/chem.201504601","journal-title":"Chem Eur J"},{"key":"10295_CR84","doi-asserted-by":"publisher","first-page":"1394","DOI":"10.1055\/s-0031-1290960","volume":"23","author":"J Zhang","year":"2012","unstructured":"J Zhang X Wang H Yu J Ye 2012 Sandmeyer-type reaction to Pinacol arylboronates in water phase: a green borylation process Synlett 23 1394 1396 https:\/\/doi.org\/10.1055\/s-0031-1290960","journal-title":"Synlett"},{"key":"10295_CR85","doi-asserted-by":"publisher","first-page":"1923","DOI":"10.1021\/jo3018878","volume":"78","author":"D Qiu","year":"2013","unstructured":"D Qiu L Jin Z Zheng H Meng F Mo X Wang Y Zhang J Wang 2013 Synthesis of Pinacol arylboronates from aromatic amines: A metal-free transformation J Org Chem 78 1923 1933 https:\/\/doi.org\/10.1021\/jo3018878","journal-title":"J Org Chem"},{"key":"10295_CR86","doi-asserted-by":"publisher","first-page":"4560","DOI":"10.1021\/ol302024m","volume":"14","author":"C Zhu","year":"2012","unstructured":"C Zhu M Yamane 2012 Transition-metal-free borylation of aryltriazene mediated by BF3. OEt2 Org Lett 14 4560 4563 https:\/\/doi.org\/10.1021\/ol302024m","journal-title":"Org Lett"},{"key":"10295_CR87","doi-asserted-by":"publisher","first-page":"2625","DOI":"10.1002\/adsc.201200416","volume":"354","author":"J Yu","year":"2012","unstructured":"J Yu L Zhang G Yan 2012 Metal-free, visible light-induced borylation of aryldiazonium salts: a simple and green synthetic route to arylboronates Adv Synth Catal 354 2625 2628 https:\/\/doi.org\/10.1002\/adsc.201200416","journal-title":"Adv Synth Catal"},{"key":"10295_CR88","doi-asserted-by":"publisher","first-page":"1702","DOI":"10.1016\/j.tetlet.2014.01.080","volume":"55","author":"LD Marciasini","year":"2014","unstructured":"LD Marciasini M Vaultier M Pucheault 2014 Borylation using group IV metallocene under mild conditions Tetrahedron Lett 55 1702 1705 https:\/\/doi.org\/10.1016\/j.tetlet.2014.01.080","journal-title":"Tetrahedron Lett"},{"key":"10295_CR89","doi-asserted-by":"publisher","first-page":"1551","DOI":"10.1016\/j.tetlet.2016.02.097","volume":"57","author":"S Ahammed","year":"2016","unstructured":"S Ahammed S Nandi D Kundu BC Ranu 2016 One-pot Suzuki coupling of aromatic amines via visible light photocatalyzed metal free borylation using t-BuONO at room temperature Tetrahedron Lett 57 1551 1554 https:\/\/doi.org\/10.1016\/j.tetlet.2016.02.097","journal-title":"Tetrahedron Lett"},{"key":"10295_CR90","doi-asserted-by":"publisher","first-page":"345","DOI":"10.1002\/open.201700036","volume":"6","author":"X Qi","year":"2017","unstructured":"X Qi L-B Jiang C Zhou J-B Peng X-F Wu 2017 Convenient and general zinc-catalyzed borylation of aryl diazonium salts and aryltriazenes under mild conditions ChemistryOpen 6 345 349 https:\/\/doi.org\/10.1002\/open.201700036","journal-title":"ChemistryOpen"},{"key":"10295_CR91","doi-asserted-by":"publisher","first-page":"2288","DOI":"10.1002\/1099-0690(200207)2002:14<2288::AID-EJOC2288>3.0.CO;2-G","volume":"2002","author":"F Bracher","year":"2002","unstructured":"F Bracher J Daab 2002 Total synthesis of the indolizidinium alkaloid ficuseptine Eur J Org Chem 2002 2288 2291 https:\/\/doi.org\/10.1002\/1099-0690(200207)2002:14<2288::AID-EJOC2288>3.0.CO;2-G","journal-title":"Eur J Org Chem"},{"key":"10295_CR92","doi-asserted-by":"publisher","first-page":"573","DOI":"10.1007\/s00706-002-0540-5","volume":"134","author":"J Daab","year":"2003","unstructured":"J Daab F Bracher 2003 Total syntheses of the alkaloids ipalbidinium and clathryimine B Monatsh Chem 134 573 583 https:\/\/doi.org\/10.1007\/s00706-002-0540-5","journal-title":"Monatsh Chem"},{"key":"10295_CR93","doi-asserted-by":"publisher","first-page":"2437","DOI":"10.1016\/j.tetlet.2005.02.047","volume":"46","author":"S-G Kim","year":"2005","unstructured":"S-G Kim J Kim H Jung 2005 Efficient total synthesis of (+)-curcuphenol via asymmetric organocatalysis Tetrahedron Lett 46 2437 2439 https:\/\/doi.org\/10.1016\/j.tetlet.2005.02.047","journal-title":"Tetrahedron Lett"},{"key":"10295_CR94","doi-asserted-by":"publisher","first-page":"7125","DOI":"10.1016\/j.tetlet.2012.10.077","volume":"53","author":"B Kandagatla","year":"2012","unstructured":"B Kandagatla VVNKVP Raju GM Reddy SC Rao J Iqbal R Bandichhor S Oruganti 2012 A facile synthesis of melatonergic antidepressant agomelatine Tetrahedron Lett 53 7125 7127 https:\/\/doi.org\/10.1016\/j.tetlet.2012.10.077","journal-title":"Tetrahedron Lett"},{"key":"10295_CR95","doi-asserted-by":"publisher","first-page":"475","DOI":"10.3184\/174751915X14381780373834","volume":"39","author":"H Liu","year":"2015","unstructured":"H Liu Y Li D Wang Y Qin M Jia 2015 An efficient synthesis of ceritinib (LDK378) using a Sandmeyer reaction J Chem Res 39 475 477 https:\/\/doi.org\/10.3184\/174751915X14381780373834","journal-title":"J Chem Res"},{"key":"10295_CR96","doi-asserted-by":"publisher","first-page":"1043","DOI":"10.1007\/s11696-018-0654-9","volume":"73","author":"Q Guo","year":"2019","unstructured":"Q Guo M Xu S Guo F Zhu Y Xie J Shen 2019 The complete synthesis of favipiravir from 2-aminopyrazine Chem Pap 73 1043 1051 https:\/\/doi.org\/10.1007\/s11696-018-0654-9","journal-title":"Chem Pap"},{"key":"10295_CR97","doi-asserted-by":"publisher","first-page":"472","DOI":"10.1023\/A:1016043608441","volume":"38","author":"TG Tsintsadze","year":"2002","unstructured":"TG Tsintsadze TE Khoshtariya LN Kurkovskaya NT Mirziashvili MI Sikharulidze 2002 Novel route for btaining isomeric benzo[b]thiophenoindoles Chem Heterocycl Compd 38 472 476 https:\/\/doi.org\/10.1023\/A:1016043608441","journal-title":"Chem Heterocycl Compd"},{"key":"10295_CR98","doi-asserted-by":"publisher","first-page":"1454","DOI":"10.1007\/s10593-005-0065-z","volume":"40","author":"TE Khoshtariya","year":"2004","unstructured":"TE Khoshtariya MM Matnadze NT Mirziashvili LN Kurkovskaya MI Sikharulidze TO Dzhashi 2004 Synthesis and reductive reactions of 2,3-dioxo-2,3-dihydrobenzo-[b]furo[2,3-f]-, -[2,3-g]-, and -[3,2-e]indoles Chem Heterocycl Compd 40 1454 1459 https:\/\/doi.org\/10.1007\/s10593-005-0065-z","journal-title":"Chem Heterocycl Compd"},{"key":"10295_CR99","doi-asserted-by":"publisher","first-page":"1111","DOI":"10.1007\/s10593-007-0171-1","volume":"43","author":"TE Khoshtariya","year":"2007","unstructured":"TE Khoshtariya LN Kurkovskaya MM Matnadze MI Sikharulidze TO Dzhashi VO Ananiashvili KT Batsikadze 2007 Condensed tetracyclic systems with an isatin fragment in the molecule Chem Heterocycl Compd 43 1111 1117 https:\/\/doi.org\/10.1007\/s10593-007-0171-1","journal-title":"Chem Heterocycl Compd"},{"key":"10295_CR100","doi-asserted-by":"publisher","first-page":"591","DOI":"10.1007\/s13726-012-0063-9","volume":"21","author":"MAK Zarchi","year":"2012","unstructured":"MAK Zarchi N Ebrahimi 2012 Facile and one-pot synthesis of aryl azides via diazotization of aromatic amine using cross-linked poly(4-vinylpyridine)-supported nitrite ion and azidation by a Sandmeyer-type reaction Iran Polym J 21 591 599 https:\/\/doi.org\/10.1007\/s13726-012-0063-9","journal-title":"Iran Polym J"},{"key":"10295_CR101","doi-asserted-by":"publisher","first-page":"330","DOI":"10.1007\/s10965-013-0330-2","volume":"21","author":"MAK Zarchi","year":"2014","unstructured":"MAK Zarchi SZ Mousavi 2014 Diazotization-bromination of aromatic amines using polymer-supported bromide via Sandmeyer-type reaction J Polym Res 21 330 338 https:\/\/doi.org\/10.1007\/s10965-013-0330-2","journal-title":"J Polym Res"},{"key":"10295_CR102","doi-asserted-by":"publisher","first-page":"6190","DOI":"10.1039\/C6SC01742H","volume":"7","author":"H Peng","year":"2016","unstructured":"H Peng R Cai C Xu H Chen X Shi 2016 Nucleophile promoted gold redox catalysis with diazonium salts: C-Br, C-S and C-P bond formation through catalytic Sandmeyer coupling Chem Sci 7 6190 6196 https:\/\/doi.org\/10.1039\/C6SC01742H","journal-title":"Chem Sci"},{"key":"10295_CR103","doi-asserted-by":"publisher","first-page":"4473","DOI":"10.1038\/s41467-020-18235-9","volume":"11","author":"X-C Gan","year":"2020","unstructured":"X-C Gan C-Y Zhang F Zhong P Tian L Yin 2020 Synthesis of chiral anti-1,2-diamine derivatives through copper(I)-catalyzed asymmetric \u03b1-addition of ketimines to aldimines Nat Commun 11 4473 4480 https:\/\/doi.org\/10.1038\/s41467-020-18235-9","journal-title":"Nat Commun"}],"container-title":["Molecular Diversity"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s11030-021-10295-3.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s11030-021-10295-3\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s11030-021-10295-3.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,9]],"date-time":"2025-04-09T09:42:10Z","timestamp":1744191730000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s11030-021-10295-3"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,8,20]]},"references-count":103,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2022,6]]}},"alternative-id":["10295"],"URL":"https:\/\/doi.org\/10.1007\/s11030-021-10295-3","relation":{},"ISSN":["1381-1991","1573-501X"],"issn-type":[{"value":"1381-1991","type":"print"},{"value":"1573-501X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2021,8,20]]},"assertion":[{"value":"23 June 2021","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"10 August 2021","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 August 2021","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare that they have no conflict of interest.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}}]}}