A new diastereoselective 3+2 annulation approach to five-membered carbocycles.

Eugene Ghera; Tamar Yechezkel; Alfred Hassner

doi:10.1016/s0040-4039(00)94468-x

A new diastereoselective 3+2 annulation approach to five-membered carbocycles.

Eugene Ghera
, Tamar Yechezkel
, Alfred Hassner

Department of Chemistry

Bar-Ilan University

Research output: Contribution to journal › Article › peer-review

28 Scopus citations

Abstract

The newly prepared 1-bromo-2-methylene-3-phenylsulfonylpropane 2 reacts with α,β unsaturated esters in a Michael induced ring closure to provide cyclopentane derivatives with complete diastereoselectivity.

Original language	English
Pages (from-to)	3653-3656
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	25
DOIs	https://doi.org/10.1016/s0040-4039(00)94468-x
State	Published - 1990

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title = "A new diastereoselective 3+2 annulation approach to five-membered carbocycles.",

abstract = "The newly prepared 1-bromo-2-methylene-3-phenylsulfonylpropane 2 reacts with α,β unsaturated esters in a Michael induced ring closure to provide cyclopentane derivatives with complete diastereoselectivity.",

author = "Eugene Ghera and Tamar Yechezkel and Alfred Hassner",

year = "1990",

doi = "10.1016/s0040-4039(00)94468-x",

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AB - The newly prepared 1-bromo-2-methylene-3-phenylsulfonylpropane 2 reacts with α,β unsaturated esters in a Michael induced ring closure to provide cyclopentane derivatives with complete diastereoselectivity.

UR - https://www.scopus.com/pages/publications/0025351297

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IS - 25

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A new diastereoselective 3+2 annulation approach to five-membered carbocycles.

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