Aminative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: a novel stereocontrolled route to substituted pyrrolidines

Literature Information

Publication Date 2004-02-24
DOI 10.1039/B316554J
Impact Factor 6.222
Authors

Alan Armstrong, Graham R. Cumming, Kurt Pike


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Abstract

Aziridination of 2-alkoxy-3,4-dihydro-2H-pyrans leads to rearrangement and stereocontrolled formation of 5-alkoxypyrrolidines which may be reduced to pyrrolidines or allylated stereoselectively.

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