The Product-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones-Reference-Cited by-同舟云学术

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The Product-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones

Published:2006-01 Issue:1 Volume:35 Page:124-125
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Sato Yoshinori,Fujisawa Hidehiko,Mukaiyama Teruaki

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference13 articles.

1. Discovery and Development of Asymmetric Autocatalysis

2. Autocatalytic Domino Michael Reaction Leading to Bicyclo[2.2.2]octane-2,5-dione Derivatives

3. Divergent stereoselectivity in the reduction of α,β-Epoxy ketones using hydridosilicates

4. Product-Catalyzed Aldol Reaction between Trimethylsilyl Enolates and Aldehydes

5. Product-catalyzed Mannich-type Reaction between Trimethylsilyl Enolates andN-Tosylaldimines

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1. The Wittig Rearrangement;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

2. Formation of Alcohols and Phenols by Ether Cleavage;Comprehensive Organic Transformations;2018-02-28

3. Development of a Phase-Transfer-Catalyzed, [2,3]-Wittig Rearrangement;The Journal of Organic Chemistry;2015-10-02

4. The [2,3]-Wittig Rearrangement;Molecular Rearrangements in Organic Synthesis;2015-10-02

5. 3.21 The Wittig Rearrangement;Comprehensive Organic Synthesis II;2014

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