Trialkylborane as an Initiator and Terminator of Free Radical Reactions. Facile Routes to Boron Enolates via α-Carbonyl Radicals and Aldol Reaction of Boron Enolates-Reference-Cited by-同舟云学术

Trialkylborane as an Initiator and Terminator of Free Radical Reactions. Facile Routes to Boron Enolates via α-Carbonyl Radicals and Aldol Reaction of Boron Enolates

Published:1991-02 Issue:2 Volume:64 Page:403-409
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Nozaki Kyoko,Oshima Koichiro,Utimoto Kiitiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/64/2/64_2_403/_pdf

Reference22 articles.

1. Organic Synthesesvia Free-Radical Displacement Reactions of Organoboranes

2. Facile reaction of organoboranes with methyl vinyl ketone. Convenient new ketone synthesis via hydroboration

3. Inhibition of the reaction of organoboranes with .alpha.,.beta.-unsaturated carbonyl derivatives by galvinoxyl. Evidence for a free-radical chain mechanism

4. New Organic Synthesis by Means of Organoboranes

5. Vinyloxyboranes as synthetic intermediates

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