化学
还原胺化
甲酸
部分
催化作用
转移加氢
胺化
氨基酸
立体选择性
组合化学
配体(生物化学)
对映选择合成
有机化学
钌
受体
生物化学
作者
Takaaki Yajima,Akito Katayama,Tsubasa Ito,Takuma Kawada,Kenya Yabushita,Toshihisa Yasuda,T. Ohta,Takeaki Katayama,Noriyuki Utsumi,Yoshihito Kayaki,Shigeki Kuwata
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-02-09
卷期号:26 (7): 1426-1431
被引量:3
标识
DOI:10.1021/acs.orglett.3c04378
摘要
A direct asymmetric reductive amination of α-keto acids catalyzed by Cp*Ir complexes bearing a chiral N-(2-picolyl)sulfonamidato ligand is described. The combined use of optically active 2-phenyglycinol as an aminating agent is effective for the chemo- and stereoselective transfer hydrogenation using formic acid. The subsequent elimination of the hydroxyethyl moiety by orthoperiodic acid can afford various unprotected α-amino acids in satisfactory isolated yields (20 examples) with excellent optical purities (up to >99% ee).
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