对映选择合成
环戊烷
化学
钯
吡咯烷
催化作用
双环分子
碱基
组合化学
有机化学
DNA
生物化学
作者
Barry M. Trost,Zhiwei Jiao,Chao‐I Hung
标识
DOI:10.1002/ange.201910061
摘要
Abstract A general method for asymmetric synthesis of heteroaryl‐containing cycles via palladium‐catalyzed cyclization is reported. Most classes of nitrogen‐containing aromatics, including pyridines, quinolines, pyrimidines, various azoles and the derivatives of nucleobases are compatible substrates, offering various heteroaryl‐substituted cyclopentane, pyrrolidine, furanidine and bicyclo[4.3.1]decadiene derivatives with good to excellent enantioselectivity and diastereoselectivity.
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