Michael Addition and Alkylation of 2-Azaallyl Anions Derived fromN-(1-Cyanoalkyl)imines, and Stereoselective Cyclization of Imine Esters or Ketones Leading to 1-Pyrrolines-Reference-Cited by-同舟云学术

Michael Addition and Alkylation of 2-Azaallyl Anions Derived fromN-(1-Cyanoalkyl)imines, and Stereoselective Cyclization of Imine Esters or Ketones Leading to 1-Pyrrolines

Published:1987-09 Issue:9 Volume:60 Page:3347-3358
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Tsuge Otohiko,Ueno Kazunori,Kanemasa Shuji,Yorozu Kiyotaka

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/60/9/60_9_3347/_pdf

Reference21 articles.

1. 1,3-Anionische Cycloadditionen von Organolithiumverbindungen; eine erste Übersicht

2. 1,3-Anionic Cycloadditions of Organolithium Compounds: An Initial Survey. New synthetic methods (4)

3. Synthetic Versatility ofN-(Silylmethyl)imines: Water-Induced Generation ofN-Protonated Azomethine Ylides of Nonstabilized Type and Fluoride-Induced Generation of 2-Azaallyl Anions

4. Regioselective cycloadditions of N-protonated azomethine ylides and 2-azaallyl anions generated from N-(silylmethyl) thioimidates, synthetic equivalents of nonstabilized nitrile ylides

5. Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalent

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