Stereoselective hetero-Claisen rearrangement of camphor derived oxazoline-N-oxides
PI Dalko, Y Langlois
Index: Dalko, Peter I.; Langlois, Yves Tetrahedron Letters, 1998 , vol. 39, # 15 p. 2107 - 2110
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Citation Number: 14
Abstract
Camphor derived oxazoline-N-oxides in the presence of various acylating agents afforded α- acyloxyoxazolines resulting from a diastereoselective [3, 3] rearrangement. The configuration of the newly formed asymmetric center was established by chemical correlation. The observed diastereoselectivity accounts a concerted rather than a stepwise process.
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