Stereoselective route to highly functionalised amino alcohols

DOI: 10.1016/0040-4039(91)85098-P

Source and publish data:

Tetrahedron Letters p. 2827 - 2828 (1991)

Update date:2022-07-29

Topics:

Authors:

Coates Coates

Malone Malone

McCarney

Stevenson

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Article abstract of DOI:10.1016/0040-4039(91)85098-P

Acyclic amino alcohols can be obtained in high stereoisomeric purity by Stevens [2,3] rearrangement of tetrahydropyridine salts followed by reduction of the ketones and ring opening of the disubstituted pyrrolidine.

Full text of DOI:10.1016/0040-4039(91)85098-P

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