Diastereoselectivity in the intramolecular cycloaddition reactions of nitrones derived from 5-alkenals and chiral hydroxylamines

DOI: 10.1016/0040-4039(91)80004-P

Source and publish data:

Tetrahedron Letters p. 4431 - 4434 (1991)

Update date:2022-08-03

Topics:

Authors:

Baldwin Baldwin

McFadyen

Aube Aube

Wilson Wilson

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Article abstract of DOI:10.1016/0040-4039(91)80004-P

Intramolecular cycloaddition of the nitrones derived from a series of 5-alkenals and α-methylbenzyl hydroxylamine leads to mixtures of diastereomeric products in the range of 1.7/1 to 16/1.

Full text of DOI:10.1016/0040-4039(91)80004-P

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