The First Tandem [2 + 2] Cycloaddition-Michael Reaction Using Ynolates: Facile Construction of Substituted Carbocycles

Mitsuru Shindo; Kenji Matsumoto; Yusuke Sato; Kozo Shishido

doi:10.1021/ol0159928

The First Tandem [2 + 2] Cycloaddition-Michael Reaction Using Ynolates: Facile Construction of Substituted Carbocycles

Mitsuru Shindo, Kenji Matsumoto, Yusuke Sato, Kozo Shishido

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

17 Citations (Scopus)

Abstract

(matrix presented) A tandem [2 + 2] cycloaddition-Michael reaction using ynolate anions followed by decarboxylation produced polysubstituted five-, six-, and seven-membered cycloalkenes.

Original language	English
Pages (from-to)	2029-2030
Number of pages	2
Journal	Organic letters
Volume	3
Issue number	13
DOIs	https://doi.org/10.1021/ol0159928
Publication status	Published - Jun 28 2001
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol0159928

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title = "The First Tandem [2 + 2] Cycloaddition-Michael Reaction Using Ynolates: Facile Construction of Substituted Carbocycles",

abstract = "(matrix presented) A tandem [2 + 2] cycloaddition-Michael reaction using ynolate anions followed by decarboxylation produced polysubstituted five-, six-, and seven-membered cycloalkenes.",

author = "Mitsuru Shindo and Kenji Matsumoto and Yusuke Sato and Kozo Shishido",

year = "2001",

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doi = "10.1021/ol0159928",

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AU - Sato, Yusuke

AU - Shishido, Kozo

PY - 2001/6/28

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AB - (matrix presented) A tandem [2 + 2] cycloaddition-Michael reaction using ynolate anions followed by decarboxylation produced polysubstituted five-, six-, and seven-membered cycloalkenes.

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