Issue 11, 1999

A Lewis acid dependent asymmetric Diels–Alder process in the cyclization of new chiral acrylamides with dienes

Abstract

Diels–Alder cycloadditions of chiral acrylamides with cyclopentadiene proceed with high diastereofacial selectivity, giving either endo-R to endo-S products depending of the Lewis acid used.

Article information

Article type
Paper

Chem. Commun., 1999, 963-964

A Lewis acid dependent asymmetric Diels–Alder process in the cyclization of new chiral acrylamides with dienes

D. Han Park, S. Han Kim, S. Min Kim, J. Dong Kim and Y. Hae Kim, Chem. Commun., 1999, 963 DOI: 10.1039/A902535I

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