Diastereoselective Alkylation Guided by Electrophile-Nucleophile ?-Interactions

DOI: 10.1021/jo00244a019

Source and publish data:

Journal of Organic Chemistry p. 1947 - 1952 (1988)

Update date:2022-09-26

Topics:

Authors:

McIntosh, John M.

Leavitt, Randy K.

Mishra, Pratibha

Cassidy, Kenneth C.

Drake, John E.

Chadha, R.

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Article abstract of DOI:10.1021/jo00244a019

Alkylation of the enolate 1a obtained from the (R)-camphor imine of tert-butyl glycinate with a variety of alkylating agents gives products whose trends in diastereomeric excesses appear to correlate with ? electron density and steric effects in the elect

Full text of DOI:10.1021/jo00244a019

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