{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,3,2]],"date-time":"2025-03-02T05:35:49Z","timestamp":1740893749977,"version":"3.38.0"},"reference-count":68,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2025,5,1]],"date-time":"2025-05-01T00:00:00Z","timestamp":1746057600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100000964","name":"ANRF","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000964","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001843","name":"Science and Engineering Research Board","doi-asserted-by":"publisher","award":["CRD\/2022\/00524"],"award-info":[{"award-number":["CRD\/2022\/00524"]}],"id":[{"id":"10.13039\/501100001843","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Carbohydrate Research"],"published-print":{"date-parts":[[2025,5]]},"DOI":"10.1016\/j.carres.2025.109435","type":"journal-article","created":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T16:09:45Z","timestamp":1740154185000},"page":"109435","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["N-nitrosamine directed stereoselective O-glycosylation reactions of 2-amino thioglycosides with NIS-TfOH"],"prefix":"10.1016","volume":"551","author":[{"given":"Vimlesh Kumar","family":"Kanaujiya","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chian-Hui","family":"Lai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3285-971X","authenticated-orcid":false,"given":"Jeyakumar","family":"Kandasamay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"year":"1982","series-title":"Occurrence and Biological Effects","author":"Loeppky","key":"10.1016\/j.carres.2025.109435_bib1"},{"key":"10.1016\/j.carres.2025.109435_bib2","series-title":"ACS (Am. Chem. Soc.) Symp. Ser.","first-page":"1","article-title":"Nitrosamines and related N-nitroso compounds: chemistry and biochemistry","volume":"Vol. 553","author":"Loeppky","year":"1994"},{"year":"2005","series-title":"Nitric Oxide Donor, for Pharmaceutical and Biological Applications","author":"Wang","key":"10.1016\/j.carres.2025.109435_bib3"},{"key":"10.1016\/j.carres.2025.109435_bib4","doi-asserted-by":"crossref","first-page":"1091","DOI":"10.1021\/cr000040l","article-title":"Nitric oxide donors: chemical activities and biological applications","volume":"102","author":"Wang","year":"2002","journal-title":"Chem. Rev."},{"key":"10.1016\/j.carres.2025.109435_bib5","doi-asserted-by":"crossref","first-page":"2485","DOI":"10.1073\/pnas.74.6.2485","article-title":"Studies of streptozotocin-induced insulitis and diabetes","volume":"74","author":"Rossini","year":"1977","journal-title":"Proc. Natl. Acad. Sci. U. S. A"},{"key":"10.1016\/j.carres.2025.109435_bib6","doi-asserted-by":"crossref","first-page":"1716","DOI":"10.7164\/antibiotics.46.1716","article-title":"Dephostatin, a novel protein tyrosine phosphatase inhibitor produced by Streptomyces II. structure determination","volume":"46","author":"Kakeya","year":"1993","journal-title":"J. Antibiot."},{"key":"10.1016\/j.carres.2025.109435_bib7","doi-asserted-by":"crossref","first-page":"829","DOI":"10.1021\/cr941192h","article-title":"A critical appraisal of the evolution of N-nitrosoureas as anticancer drugs","volume":"97","author":"Gnewuch","year":"1997","journal-title":"Chem. Rev."},{"key":"10.1016\/j.carres.2025.109435_bib8","doi-asserted-by":"crossref","first-page":"506","DOI":"10.1021\/cb200440y","article-title":"First-in-class small molecule inhibitors of the single-strand DNA cytosine deaminase APOBEC3G","volume":"7","author":"Li","year":"2012","journal-title":"ACS Chem. Biol."},{"year":"2004","series-title":"Principles and Management of Cancer","author":"Sen","key":"10.1016\/j.carres.2025.109435_bib9"},{"key":"10.1016\/j.carres.2025.109435_bib10","doi-asserted-by":"crossref","first-page":"497","DOI":"10.7164\/antibiotics.25.497","article-title":"Dopastin, an inhibitor of dopamine \u03b2-hydroxylase","volume":"25","author":"Iinuma","year":"1972","journal-title":"J. Antibiot."},{"key":"10.1016\/j.carres.2025.109435_bib11","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1021\/bk-1979-0101.ch001","article-title":"N-Nitrosamines","volume":"101","author":"Anselme","year":"1979","journal-title":"ACS Symp. Ser."},{"key":"10.1016\/j.carres.2025.109435_bib12","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1080\/00304948709356181","article-title":"Recent synthetic applications of N-nitrosamines and related compounds","volume":"19","author":"Saavedra","year":"1987","journal-title":"Org. Prep. Proced. Int."},{"key":"10.1016\/j.carres.2025.109435_bib13","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1016\/0040-4020(82)80184-1","article-title":"Metal-assisted reactions\u2014Part 11: rapid reduction of N-nitrosamines to N, N-disubstituted hydrazines the utility of some low-valent titanium reagents","volume":"38","author":"Entwistle","year":"1982","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_bib14","doi-asserted-by":"crossref","first-page":"2112","DOI":"10.1021\/ja01128a514","article-title":"A curarimimetic analog of decamethylene ditrimethylammonium (C10)","volume":"74","author":"Schueler","year":"1952","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.carres.2025.109435_bib15","doi-asserted-by":"crossref","first-page":"66","DOI":"10.15227\/orgsyn.013.0066","article-title":"\u03b1-Methyl-\u03b1-phenylhydrazine","volume":"13","author":"Hartman","year":"1933","journal-title":"Org. Synth."},{"key":"10.1016\/j.carres.2025.109435_bib16","doi-asserted-by":"crossref","first-page":"529","DOI":"10.1021\/jo01098a007","article-title":"Synthesis of some 1, 1-dibenzylhydrazines1","volume":"23","author":"Hinman","year":"1958","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib17","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1016\/j.tet.2009.10.085","article-title":"Recent developments in the chemistry of sydnones","volume":"66","author":"Browne","year":"2010","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_sref18","doi-asserted-by":"crossref","first-page":"129","DOI":"10.1021\/cr60228a004","article-title":"The chemistry of the sydnones","volume":"64","author":"Stewart","year":"1964","journal-title":"Chem. Rev."},{"key":"10.1016\/j.carres.2025.109435_bib18i","doi-asserted-by":"crossref","first-page":"1343","DOI":"10.1016\/0040-4020(75)80181-5","article-title":"The mechanism of the Fischer-Hepp rearrangement of aromatic N-nitroso-amines","volume":"31","author":"Williams","year":"1975","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_bib19","doi-asserted-by":"crossref","first-page":"1819","DOI":"10.3762\/bjoc.9.212","article-title":"The first example of the Fischer\u2013Hepp type rearrangement in pyrimidines","volume":"9","author":"Cikotiene","year":"2013","journal-title":"Beilstein J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib20","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1002\/anie.197500151","article-title":"Umpolung of amine reactivity. Nucleophilic \u03b1\u2010(secondary amino)\u2010alkylation via metalated nitrosamines","volume":"14","author":"Seebach","year":"1975","journal-title":"Angew. Chem., Int. Ed. Engl."},{"key":"10.1016\/j.carres.2025.109435_bib21","doi-asserted-by":"crossref","first-page":"8481","DOI":"10.1021\/acs.chemrev.7b00307","article-title":"Introduction: CH activation","volume":"117","author":"Crabtree","year":"2017","journal-title":"Chem. Rev."},{"key":"10.1016\/j.carres.2025.109435_bib22","doi-asserted-by":"crossref","first-page":"10236","DOI":"10.1002\/anie.201203269","article-title":"Beyond directing groups: transition\u2010metal\u2010catalyzed C-H activation of simple arenes","volume":"51","author":"Kuhl","year":"2012","journal-title":"Angew. Chem., Int. Ed. Engl."},{"key":"10.1016\/j.carres.2025.109435_bib23","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1021\/ja3099245","article-title":"Rhodium (III)-catalyzed N-nitroso-directed C\u2013H olefination of arenes. High-yield, versatile coupling under mild conditions","volume":"135","author":"Liu","year":"2013","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.carres.2025.109435_bib24","doi-asserted-by":"crossref","first-page":"16625","DOI":"10.1021\/ja408541c","article-title":"Rhodium (III)-catalyzed indole synthesis using N\u2013N bond as an internal oxidant","volume":"135","author":"Liu","year":"2013","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.carres.2025.109435_bib25","doi-asserted-by":"crossref","first-page":"5294","DOI":"10.1021\/ol402523x","article-title":"Traceless directing strategy: efficient synthesis of N-alkyl indoles via redox-neutral C\u2013H activation","volume":"15","author":"Wang","year":"2013","journal-title":"Org. Lett."},{"key":"10.1016\/j.carres.2025.109435_bib26","doi-asserted-by":"crossref","first-page":"14245","DOI":"10.1002\/chem.201404506","article-title":"Rhodium (III)\u2010Catalyzed N\u2010Nitroso\u2010Directed C-H addition to ethyl 2\u2010oxoacetate for cycloaddition\/fragmentation synthesis of indazoles","volume":"20","author":"Chen","year":"2014","journal-title":"Chem. Eur J."},{"key":"10.1016\/j.carres.2025.109435_bib27","doi-asserted-by":"crossref","first-page":"9888","DOI":"10.1021\/jo501902d","article-title":"Palladium-catalyzed N-Nitroso-Directed C\u2013H alkoxylation of arenes and subsequent formation of 2-alkoxy-N-alkylarylamines","volume":"79","author":"Gao","year":"2014","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib28","doi-asserted-by":"crossref","first-page":"15352","DOI":"10.1039\/C4CC07440H","article-title":"Palladium-catalyzed oxidative C\u2013H bond acylation of N-nitrosoanilines with toluene derivatives: a traceless approach to synthesize N-alkyl-2-aminobenzophenones","volume":"50","author":"Wu","year":"2014","journal-title":"Chem. Commun."},{"key":"10.1016\/j.carres.2025.109435_bib29","doi-asserted-by":"crossref","first-page":"4780","DOI":"10.1021\/ja501910e","article-title":"Rh (III)-and Ir (III)-catalyzed C\u2013H alkynylation of arenes under chelation assistance","volume":"136","author":"Xie","year":"2014","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.carres.2025.109435_bib30","doi-asserted-by":"crossref","first-page":"1200","DOI":"10.1021\/ol5000764","article-title":"Rhodium (III)-catalyzed C\u2013C coupling of arenes with 2-vinyloxiranes: synthesis of allylic alcohols","volume":"16","author":"Yu","year":"2014","journal-title":"Org. Lett."},{"key":"10.1016\/j.carres.2025.109435_bib31","doi-asserted-by":"crossref","first-page":"6958","DOI":"10.1039\/C5OB00691K","article-title":"Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp 2 C\u2013H bond activation","volume":"13","author":"Li","year":"2015","journal-title":"Org. Biomol. Chem."},{"year":"1999","series-title":"Essentials of Glycobiology","author":"Varki","key":"10.1016\/j.carres.2025.109435_bib32"},{"year":"2008","series-title":"Essentials of Carbohydrate Chemistry and Biochemistry","author":"Lindhorst","key":"10.1016\/j.carres.2025.109435_bib33"},{"key":"10.1016\/j.carres.2025.109435_bib34","doi-asserted-by":"crossref","first-page":"1046","DOI":"10.1038\/nature05819","article-title":"Synthesis and medical applications of oligosaccharides","volume":"446","author":"Seeberger","year":"2007","journal-title":"Nature"},{"key":"10.1016\/j.carres.2025.109435_bib35","doi-asserted-by":"crossref","first-page":"751","DOI":"10.1038\/nrd1823","article-title":"Automated synthesis of oligosaccharides as a basis for drug discovery","volume":"4","author":"Seeberger","year":"2005","journal-title":"Nat. Rev. Drug Discov."},{"year":"2017","series-title":"Selective Glycosylations: Synthetic Methods and Catalysts","author":"Bennett","key":"10.1016\/j.carres.2025.109435_bib36"},{"year":"2014","series-title":"Modern Synthetic Methods in Carbohydrate Chemistry: from Monosaccharides to Complex Glycoconjugates","author":"Werz","key":"10.1016\/j.carres.2025.109435_bib37"},{"year":"1996","series-title":"Modern Methods in Carbohydrate Synthesis","author":"Khan","key":"10.1016\/j.carres.2025.109435_bib38"},{"key":"10.1016\/j.carres.2025.109435_bib39","doi-asserted-by":"crossref","first-page":"4423","DOI":"10.1021\/cr990307k","article-title":"Intramolecular O-glycoside bond formation","volume":"100","author":"Jung","year":"2000","journal-title":"Chem. Rev."},{"key":"10.1016\/j.carres.2025.109435_bib40","doi-asserted-by":"crossref","first-page":"1900","DOI":"10.1002\/anie.200802036","article-title":"New principles for glycoside\u2010bond formation","volume":"48","author":"Zhu","year":"2009","journal-title":"Angew. Chem., Int. Ed. Engl."},{"year":"2008","series-title":"Handbook of Chemical Glycosylation: Advances in Stereoselectivity and Therapeutic Relevance","key":"10.1016\/j.carres.2025.109435_bib41"},{"key":"10.1016\/j.carres.2025.109435_bib42","doi-asserted-by":"crossref","first-page":"3596","DOI":"10.1039\/c004281a","article-title":"Recent advances in stereoselective glycosylation through intramolecular aglycon delivery","volume":"8","author":"Ishiwata","year":"2010","journal-title":"Org. Biomol. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib43","doi-asserted-by":"crossref","first-page":"14431","DOI":"10.1002\/anie.201606774","article-title":"Nucleophile\u2010directed stereocontrol over glycosylations using geminal\u2010difluorinated nucleophiles","volume":"55","author":"Schumann","year":"2016","journal-title":"Angew. Chem., Int. Ed. Engl."},{"key":"10.1016\/j.carres.2025.109435_bib44","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1016\/bs.accb.2016.08.001","article-title":"Recent advances toward robust N-protecting groups for glucosamine as required for glycosylation strategies","volume":"73","author":"Aly","year":"2016","journal-title":"Adv. Carbohydr. Chem. Biochem."},{"key":"10.1016\/j.carres.2025.109435_bib45","doi-asserted-by":"crossref","first-page":"2323","DOI":"10.1039\/C5GC02880A","article-title":"An efficient synthesis of N-nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite","volume":"18","author":"Chaudhary","year":"2016","journal-title":"Green Chem."},{"key":"10.1016\/j.carres.2025.109435_bib46","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1021\/acs.joc.8b02377","article-title":"Regioselective nitration of N-alkyl anilines using tert-butyl nitrite under mild condition","volume":"84","author":"Chaudhary","year":"2018","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib47","doi-asserted-by":"crossref","first-page":"6215","DOI":"10.1039\/C6GC02444K","article-title":"A metal free reduction of aryl-N-nitrosamines to the corresponding hydrazines using a sustainable reductant thiourea dioxide","volume":"18","author":"Chaudhary","year":"2016","journal-title":"Green Chem."},{"key":"10.1016\/j.carres.2025.109435_bib48","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1002\/adsc.201701047","article-title":"An efficient metal\u2010free method for the denitrosation of aryl N\u2010nitrosamines at room temperature","volume":"360","author":"Chaudhary","year":"2018","journal-title":"Adv. Synth. Catal."},{"key":"10.1016\/j.carres.2025.109435_bib49","doi-asserted-by":"crossref","first-page":"845","DOI":"10.1039\/C8OB03010C","article-title":"tert-Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions","volume":"17","author":"Sureshbabu","year":"2019","journal-title":"Org. Biomol. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib50","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1016\/j.tetlet.2017.12.033","article-title":"tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature","volume":"59","author":"Chauhan","year":"2018","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_bib51","doi-asserted-by":"crossref","first-page":"8280","DOI":"10.1039\/C8OB01950A","article-title":"tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature","volume":"16","author":"Azeez","year":"2018","journal-title":"Org. Biomol. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib52","article-title":"Palladium\u2010catalyzed reaction of aryl iodides and glycal enones: application in the preparation of dapagliflozin analogues","volume":"33","author":"Kumar Singh","year":"2022","journal-title":"Eur. J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib53","doi-asserted-by":"crossref","first-page":"7650","DOI":"10.1021\/acs.orglett.0c02843","article-title":"Development of routes for the stereoselective preparation of \u03b2-aryl-C-glycosides via C-1 aryl enones","volume":"22","author":"Singh","year":"2020","journal-title":"Org. Lett."},{"key":"10.1016\/j.carres.2025.109435_bib54","doi-asserted-by":"crossref","first-page":"549","DOI":"10.1002\/ajoc.201900055","article-title":"Tris (Pentafluorophenyl) Borane\u2010Driven stereoselective O\u2010glycosylation with glycal donors under mild condition","volume":"8","author":"Mishra","year":"2019","journal-title":"Asian J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib55","doi-asserted-by":"crossref","first-page":"5107","DOI":"10.1039\/C8OB01393D","article-title":"Palladium catalyzed stereocontrolled synthesis of C-aryl glycosides using glycals and arenediazonium salts at room temperature","volume":"16","author":"Singh","year":"2018","journal-title":"Org. Biomol. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib56","doi-asserted-by":"crossref","first-page":"4204","DOI":"10.1021\/acs.joc.8b00215","article-title":"Tris (pentafluorophenyl) borane-promoted stereoselective glycosylation with glycosyl trichloroacetimidates under mild conditions","volume":"83","author":"Mishra","year":"2018","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib57","doi-asserted-by":"crossref","DOI":"10.1016\/j.tetlet.2022.153852","article-title":"An efficient and direct esterification of uronic acids using H2SO4-SiO2 at room temperature","volume":"99","author":"Tiwari","year":"2022","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_bib58","doi-asserted-by":"crossref","first-page":"3859","DOI":"10.1039\/C9QO01010F","article-title":"Synthesis of photolabile protecting group (PPG) protected uronic acid building blocks: applications in carbohydrate synthesis with the assistance of a continuous flow photoreactor","volume":"6","author":"Tiwari","year":"2019","journal-title":"Org. Chem. Front."},{"key":"10.1016\/j.carres.2025.109435_bib59","doi-asserted-by":"crossref","first-page":"2511","DOI":"10.1016\/j.tetlet.2018.05.021","article-title":"A highly efficient TEMPO mediated oxidation of sugar primary alcohols into uronic acids using 1-chloro-1, 2-benziodoxol-3 (1H)-one at room temperature","volume":"59","author":"Tiwari","year":"2018","journal-title":"Tetrahedron Lett."},{"key":"10.1016\/j.carres.2025.109435_bib60","doi-asserted-by":"crossref","first-page":"11414","DOI":"10.1021\/acs.joc.2c00930","article-title":"Copper (I)-catalyzed sandmeyer-type S-arylation of 1-thiosugars with aryldiazonium salts under mild conditions","volume":"87","author":"Venkatesh","year":"2022","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib61","doi-asserted-by":"crossref","DOI":"10.1002\/ajoc.202200315","article-title":"Synthesis of glycouronamides by transamidation approach at room temperature","volume":"11","author":"Kanaujiya","year":"2022","journal-title":"Asian J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib62","series-title":"General Carbohydrate Method","first-page":"282","article-title":"2-Acetamido-3, 4, 6-tri-O-acetyl-2-deoxy-\u03b1-d-glucopyranosyl chloride","author":"Horton","year":"1972"},{"issue":"11","key":"10.1016\/j.carres.2025.109435_bib63","doi-asserted-by":"crossref","first-page":"2163","DOI":"10.1016\/S0957-4166(00)86292-8","article-title":"Dibutylstannylene acetals: useful intermediates for the regioselective sulfation of glycosides","volume":"5","author":"Guilbert","year":"1994","journal-title":"Tetrahedron Asymmetry"},{"key":"10.1016\/j.carres.2025.109435_bib64","doi-asserted-by":"crossref","first-page":"872","DOI":"10.1016\/j.carres.2010.02.013","article-title":"Direct chemical glycosylation with pentenyl-and thioglycoside donors of N-acetylglucosamine","volume":"7","author":"Krag","year":"2010","journal-title":"Carbohydr. Res."},{"key":"10.1016\/j.carres.2025.109435_bib65","doi-asserted-by":"crossref","first-page":"3502","DOI":"10.1021\/jo1023156","article-title":"Glucosamine-based primary amines as organocatalysts for the asymmetric aldol reaction","volume":"9","author":"Agarwal","year":"2011","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.carres.2025.109435_bib66","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1021\/ol102750h","article-title":"One-pot azidochlorination of glycals","volume":"4","author":"Plattner","year":"2011","journal-title":"Org. Lett."},{"key":"10.1016\/j.carres.2025.109435_bib67","doi-asserted-by":"crossref","first-page":"1434","DOI":"10.1021\/acs.joc.9b02396","article-title":"Positional scanning MUC1 glycopeptide library reveals the importance of PDTR epitope glycosylation for lectin binding","volume":"85","author":"Singh","year":"2019","journal-title":"J. Org. Chem."}],"container-title":["Carbohydrate Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0008621525000618?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0008621525000618?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,3,1]],"date-time":"2025-03-01T09:29:17Z","timestamp":1740821357000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0008621525000618"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,5]]},"references-count":68,"alternative-id":["S0008621525000618"],"URL":"https:\/\/doi.org\/10.1016\/j.carres.2025.109435","relation":{},"ISSN":["0008-6215"],"issn-type":[{"type":"print","value":"0008-6215"}],"subject":[],"published":{"date-parts":[[2025,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"N-nitrosamine directed stereoselective O-glycosylation reactions of 2-amino thioglycosides with NIS-TfOH","name":"articletitle","label":"Article Title"},{"value":"Carbohydrate Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.carres.2025.109435","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2025 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}],"article-number":"109435"}}