"Extension of β-chloroenals to ethyl 5-chloro-2,4-pentadienoates using Wadsworth–Emmons reactions: subsequent conversions to 5-aryl-5-chloro-2,4-pentadienoic acids and 5-aryl-2-penten-4-ynoic acids" by Seann P. Mulcahy

Article

Extension of β-chloroenals to ethyl 5-chloro-2,4-pentadienoates using Wadsworth–Emmons reactions: subsequent conversions to 5-aryl-5-chloro-2,4-pentadienoic acids and 5-aryl-2-penten-4-ynoic acids

Tetrahedron (2004)

Seann P. Mulcahy, Providence College

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Abstract

Convenient routes from (Z)-3-aryl-3-chloroenals to (2E,4Z)-5-aryl-5-chloro-2,4-pentadienoates and (2E)-5-aryl-2-penten-4-ynoates are described. The stereochemical assignments are based on NMR spectral data.

Disciplines

Chemistry

Publication Date

November 1, 2004

Citation Information

Seann P. Mulcahy. "Extension of β-chloroenals to ethyl 5-chloro-2,4-pentadienoates using Wadsworth–Emmons reactions: subsequent conversions to 5-aryl-5-chloro-2,4-pentadienoic acids and 5-aryl-2-penten-4-ynoic acids" Tetrahedron Vol. 60 Iss. 45 (2004)
Available at: http://works.bepress.com/seann_mulcahy/4/