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 journalArticlepeer-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 languageEnglish
Pages (from-to)2029-2030
Number of pages2
JournalOrganic letters
Volume3
Issue number13
DOIs
Publication statusPublished - Jun 28 2001
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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