Bicycloannulation of C=N Double Bonds through Organotin-Aided Three Component Coupling. A Short and Stereoselective Synthesis of (±)-allo-Berbane and (±)-allo-Yohimbane Systems-Reference-Cited by-同舟云学术

Bicycloannulation of C=N Double Bonds through Organotin-Aided Three Component Coupling. A Short and Stereoselective Synthesis of (±)-allo-Berbane and (±)-allo-Yohimbane Systems

Published:1990-12 Issue:12 Volume:19 Page:2161-2164
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yamaguchi Ryohei,Hamasaki Takashi,Utimoto Kiitiro,Kozima Sinpei,Takaya Hidemasa

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/19/12/19_12_2161/_pdf

Reference17 articles.

1. Highly regioselective .alpha.-allylation of N-(alkoxycarbonyl)pyridinium salts by means of allyltin reagents

2. Highly regio- and chemo-selective γ-addition of benzylic group to N-alkoxycarbonylpyridiniuin salts by means of organotin reagent

3. Regio- and chemoselective addition of alkynyltin reagents to the 2-position of 3-acylpyridines activated by methyl chloroformate: selective synthesis of 2,3-disubstituted 1,2-dihydropyridines

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