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Scientific article
English

A model for the stereoselectivity of radical mediated reductive alkylation of acyclic enamines

Published inSynlett, no. 3, p. 211-213
Publication date1992
Abstract

The radical mediated reductive alkylation of enamines [e.g., (E)-1-phenyl-1-pyrrolidino-1-propene (1)] derived from propiophenone is investigated. The observed stereoselectivities are explained with a model based on semiempirical calculations of the radical intermediate conformation

Affiliation Not a UNIGE publication
Citation (ISO format)
RENAUD, P. et al. A model for the stereoselectivity of radical mediated reductive alkylation of acyclic enamines. In: Synlett, 1992, n° 3, p. 211–213. doi: 10.1055/s-1992-21316
Identifiers
ISSN of the journal0936-5214
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