High diastereofacial selectivity in the 1,3-dipolar cycloaddition of chiral azomethine ylides

DOI: 10.1016/S0957-4166(00)80019-1

Source and publish data:

Tetrahedron Asymmetry p. 1189 - 1192 (1991)

Update date:2022-08-04

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Authors:

Deprez Deprez

Royer Royer

Husson Husson

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Article abstract of DOI:10.1016/S0957-4166(00)80019-1

Excellent diastereofacial and endo/exo stereoselectivities have been obtained in cycloaddition of the chiral azomethine ylide generated from 4-phenyloxazolidine acetic acid (-)-8-phenylmenthyl ester 1e.

Full text of DOI:10.1016/S0957-4166(00)80019-1

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Product name:((R)-4-Phenyl-oxazolidin-3-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

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