Diastereoselection in the conjugate additions of organocopper reagents to N-enoyloxazolidinones

DOI: 10.1016/S0040-4039(98)01966-2

Source and publish data:

Tetrahedron Letters p. 8593 - 8596 (1998)

Update date:2022-08-05

Topics:

Authors:

Williams, David R.

Kissel, William S.

Li, Jie Jack

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Article abstract of DOI:10.1016/S0040-4039(98)01966-2

A survey of conjugate additions of Yamamoto organocopper reagents to N- enoyl-4-substituted oxazolidinones is reported. Diastereofacial selectivity is reversed for 4-phenyl and 4-benzyloxazolidinones of the same relative configuration. Alkenylcopper reage

Full text of DOI:10.1016/S0040-4039(98)01966-2

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