烷基化
化学
吡咯烷
对映选择合成
铱
催化作用
阳离子聚合
有机化学
药物化学
作者
Daisuke Yamauchi,Kentaro Yamakawa,Takahiro Nishimura
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-09-15
卷期号:24 (37): 6828-6833
被引量:4
标识
DOI:10.1021/acs.orglett.2c02733
摘要
Enantioselective direct α-C(sp3)-H alkylation of saturated cyclic amines having N-methylbenzimidazolyl as a directing group was realized by using a cationic iridium/chiral diphosphine catalyst. The alkylation of pyrrolidine derivatives with various terminal alkenes proceeded to give α-alkylated products in high yields with high enantioselectivities. Chiral α,α'-dialkylated pyrrolidine derivatives were also synthesized by using an excess of alkenes or by stepwise alkylation.
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