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钯(II)催化由(Z)-N-烯丙基2-炔酰胺不对称合成(Z)-α-亚烷基-γ-丁内酰胺。(-)-异辛诺米定的全合成。

Palladium(II)-catalyzed asymmetric synthesis of (Z)-alpha-alkylidene-gamma-butyrolactams from (Z)-N-allylic 2-Alkynamides. Total synthesis of (-)-isocynometrine.

作者信息

Xu Wei, Kong Aidi, Lu Xiyan

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai, 200032, China.

出版信息

J Org Chem. 2006 May 12;71(10):3854-8. doi: 10.1021/jo060288w.

Abstract

Pd(OAc)2 combined with nitrogen-containing ligands catalyzed the cyclization of (Z)-N-allylic 2-alkynamides in acetic acid to afford the alpha-(Z)-acetoxyalkylidene-gamma-butyrolactams in high yield and high stereoselectivity. When chiral nitrogen-containing ligands were used, the catalytic asymmetric protocol was achieved with moderate enantioselectivity (up to 80 degrees C). The utility of this new methodology was exemplified by the total synthesis of (-)-isocynometrine.

摘要

醋酸钯与含氮配体相结合,在醋酸中催化(Z)-N-烯丙基-2-炔酰胺的环化反应,以高产率和高立体选择性得到α-(Z)-乙酰氧基亚烷基-γ-丁内酰胺。当使用手性含氮配体时,可实现具有中等对映选择性的催化不对称反应(高达80℃)。(-)-异辛诺明的全合成例证了这种新方法的实用性。

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