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The first tandem [2 + 2] cycloaddition--Michael reaction using ynolates: facile construction of substituted
M Shindo1, K Matsumoto, Y Sato
1Institute for Medicinal Resources, University of Tokushima, and TOREST, Japan. shindo@fc.ph2.tokushima-u.ac.jp
Organic Letters
|June 22, 2001
Abstract:
[reaction: see text] A tandem [2 + 2] cycloaddition-Michael reaction using ynolate anions followed by decarboxylation produced polysubstituted five-, six-, and seven-membered cycloalkenes.