Stereoselective approaches to trisubstituted pyrrolidines

DOI: 10.1016/S0040-4039(00)97620-2

Source and publish data:

Tetrahedron Letters p. 4351 - 4354 (1990)

Update date:2022-08-03

Topics:

Authors:

Burns Burns

Coates Coates

Neeson Neeson

Stevenson

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Article abstract of DOI:10.1016/S0040-4039(00)97620-2

5,6-Alkyl substituted 1,2,5,6-tetrahydropyridine salts undergo Stevens [3,2] rearrangement with ring contraction to give 2,3,4 or 2,3,5-trisubstituted pyrrolidines with 100% stereoselectivity.

Full text of DOI:10.1016/S0040-4039(00)97620-2

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