对映选择合成
亲核细胞
催化作用
化学
组合化学
有机化学
作者
Lunfeng Chen,Pengfei Li
标识
DOI:10.1002/slct.202304866
摘要
Abstract With chiral amine (DHQD) 2 PHAL as nucleophilic catalyst, asymmetric synthesis of enantioenriched 3‐allylindoles was achieved from indolone‐2‐imines and MBH carbonates. Compared with our previous chiral phosphine catalysis, the chiral amine had exactly the opposite effect in terms of enantioselectivity. Importantly, we could obtain each enantiomer by adjusting the catalyst system.
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