{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T11:08:25Z","timestamp":1790420905202,"version":"4.1.0"},"reference-count":49,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,7,24]],"date-time":"2026-07-24T00:00:00Z","timestamp":1784851200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,7,24]],"date-time":"2026-07-24T00:00:00Z","timestamp":1784851200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100004543","name":"China Scholarship Council","doi-asserted-by":"publisher","award":["202306890033"],"award-info":[{"award-number":["202306890033"]}],"id":[{"id":"10.13039\/501100004543","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chemistry A European J"],"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    The preparation of a series of enantioenriched \u03b1\u2010substituted primary amines using rhodium\u2010catalyzed asymmetric transfer hydrogenation of\n                    <jats:italic>ortho\u2010<\/jats:italic>\n                    hydroxyaryl N\u2500H imines is reported. The reaction proceeds under mild conditions using a low catalyst loading and ammonium formate as the hydrogen source, delivering the reduced compounds in high yields (up to 99%) and enantioselectivities (up to 99% ee).\n                  <\/jats:p>","DOI":"10.1002\/chem.71466","type":"journal-article","created":{"date-parts":[[2026,7,25]],"date-time":"2026-07-25T01:29:12Z","timestamp":1784942952000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Rhodium\u2010Catalyzed Synthesis of Enantioenriched \u03b1\u2010Substituted Primary Amines Through Asymmetric Transfer Hydrogenation"],"prefix":"10.1002","author":[{"given":"Chonghuo","family":"Liu","sequence":"first","affiliation":[{"name":"Institute of Chemistry for Life and Health Sciences CNRS, CSB2D Team  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9409-5861","authenticated-orcid":false,"given":"Guillaume","family":"Lef\u00e8vre","sequence":"additional","affiliation":[{"name":"Institute of Chemistry for Life and Health Sciences CNRS, CSB2D Team  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3534-3786","authenticated-orcid":false,"given":"Qin","family":"Yin","sequence":"additional","affiliation":[{"name":"Faculty of Pharmaceutical Sciences Shenzhen University of Advanced Technology  Shenzhen Guangdong China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Phannarath","family":"Phansavath","sequence":"additional","affiliation":[{"name":"Institute of Chemistry for Life and Health Sciences CNRS, CSB2D Team  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1167-1195","authenticated-orcid":false,"given":"Virginie","family":"Ratovelomanana\u2010Vidal","sequence":"additional","affiliation":[{"name":"Institute of Chemistry for Life and Health Sciences CNRS, CSB2D Team  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,7,24]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"crossref","DOI":"10.1002\/9783527826186","volume-title":"Methodologies in Amine Synthesis: Challenges and Applications","author":"Ricci A.","year":"2021"},{"key":"e_1_2_7_3_1","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1055\/s-0032-1317589","article-title":"Step\u2010Efficient Access to Chiral Primary Amines","volume":"45","author":"Nugent T. 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