Alkali metal hydride or aqueous hydroxide induced conjugate addition of trimethylsilyl enol ethers to enones. A convenient alternative to Lewis acid mediated reaction-Reference-Cited by-同舟云学术

Alkali metal hydride or aqueous hydroxide induced conjugate addition of trimethylsilyl enol ethers to enones. A convenient alternative to Lewis acid mediated reaction

Published:1998-03 Issue:10 Volume:39 Page:1261-1264
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Swamy Vishwanath M.,Sarkar Amitabha

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. THE NEW MICHAEL REACTION

2. The Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Eetones and Acetals in the Presence of Titanium Tetraalkoxide and Titanium Tetrachloride

3. THE MICHAEL TYPE REACTION OF O-SILYLATED KETENE ACETALS WITH α,β-UNSATURATED CARBONYL COMPOUNDS PROMOTED BY TITANIUM TETRACHLORIDE

4. Titanium Tetrachloride in Organic Synthesis[New synthetic methods(21)]

5. Total synthesis of dl-quadrone

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