Modified Wittig Reactions Using Triethylamine and Lithium Halides: Synthesis of α,β-Unsaturated Esters from Ketones and Ethyl Bis(Trifluoroethyl)Phosphonoacetate-Reference-Cited by-同舟云学术

Modified Wittig Reactions Using Triethylamine and Lithium Halides: Synthesis of α,β-Unsaturated Esters from Ketones and Ethyl Bis(Trifluoroethyl)Phosphonoacetate

Published:1990-03 Issue:6 Volume:20 Page:869-875
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Rathke Michael W.¹,Bouhlel Ezzeddine¹

Affiliation:

1. a Department of Chemistry , Michigan State University , East Lansing, Michigan, 48824

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397919008052333

Reference5 articles.

1. Wadswortb , W. S. Jr. 1977. Organic Reactions, Vol. 25, 73–254. New York: Wiley.

2. The Horner-Wadsworth-Emmons modification of the Wittig reaction using triethylamine and lithium or magnesium salts

3. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.

4. A Highly Selective Synthesis of a Chiral Gamma-amino Trisubstituted Z-Vinyl Ester.1

5. New Methods for Synthesis of α,β-Unsaturated Carboxylic Esters from Carbonyl Compounds Using Monoanions of Dithiocarbonates, and Dianions of Ethyl Mercaptoacetate and Ethyl 2-Mercaptopropionate

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