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Asymmetric Stepwise Reductive Amination of Aryl N-Heteroaryl Ketones with Benzyl Amines via Iridium Catalysis
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2021-09-15 , DOI: 10.1002/ajoc.202100472 Bing Yang 1 , Hao Fu 2 , Jing Yuan 3 , Simiaomiao Wen 2 , Chunqin Wang 4 , Qixing Liu 2 , Haifeng Zhou 5
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2021-09-15 , DOI: 10.1002/ajoc.202100472 Bing Yang 1 , Hao Fu 2 , Jing Yuan 3 , Simiaomiao Wen 2 , Chunqin Wang 4 , Qixing Liu 2 , Haifeng Zhou 5
Affiliation
Various chiral aryl N-heteroaryl methylamines were prepared with good yields and up to 99% enantioselectivity via one-pot stepwise ketimine formation/asymmetric transfer hydrogenation of aryl N-heteroaryl ketones and benzyl amines.
中文翻译:
通过铱催化不对称逐步还原胺化芳基 N-杂芳基酮与苄胺
通过芳基 N-杂芳基酮和苄基胺的一锅逐步酮亚胺形成/不对称转移氢化,制备了各种手性芳基 N-杂芳基甲胺,收率高,对映选择性高达 99%。
更新日期:2021-11-15
中文翻译:
通过铱催化不对称逐步还原胺化芳基 N-杂芳基酮与苄胺
通过芳基 N-杂芳基酮和苄基胺的一锅逐步酮亚胺形成/不对称转移氢化,制备了各种手性芳基 N-杂芳基甲胺,收率高,对映选择性高达 99%。