The first tandem [2+2] cycloaddition-Michael reaction using ynolates: Facile construction of substituted carbocycles

Authors
Shindo, M Matsumoto, K Sato, Y Shishido, K
Citation
M. Shindo et al., The first tandem [2+2] cycloaddition-Michael reaction using ynolates: Facile construction of substituted carbocycles, ORG LETT, 3(13), 2001, pp. 2029-2031
Citations number
25
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
13
Year of publication
2001
Pages
2029 - 2031
Database
ISI
SICI code
1523-7060(20010628)3:13<2029:TFT[CR>2.0.ZU;2-0
Abstract
[GRAPHICS] A tandem [2 + 2] cycloaddition-Michael reaction using ynolate anions follow ed by decarboxylation produced polysubstituted five-, six-, and seven-membe red cycloalkenes.