Issue 11, 1999
From the journal:

Chemical Communications

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

Doo Han Park,   Sung Han Kim,   Sam Min Kim,   Jin Dong Kim  and  Yong Hae Kim  

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.

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Article information

DOI
https://doi.org/10.1039/A902535I
Article type
Paper

Chem. Commun., 1999, 963-964

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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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