A tandem ester cleavage-Michael addition reaction for the synthesis of oxygen heterocycles

Article abstract of DOI:10.1080/00397919308013298

A tandem ester cleavage-Michael addition sequence has been developed for the preparation of five- and six-ring oxygen heterocycles bearing an acetic acid residue at C-2. Treatment of ethyl 6- or 7-acetyloxy-2-alkenoates with ethanolic sodium ethoxide affo

Full text of DOI:10.1080/00397919308013298

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Tandem Ester Cleavage-
Michael Addition Reaction
for the Synthesis of Oxygen
Heterocycles
R. A. Bunce a & M. J. Bennett a
a Department of Chemistry, Oklahoma State
University Stillwater, OK, 74078-0447, USA
Version of record first published: 23 Sep 2006
To cite this article: R. A. Bunce & M. J. Bennett (1993): A Tandem Ester Cleavage-
Michael Addition Reaction for the Synthesis of Oxygen Heterocycles, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:7, 1009-1020
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