A model for the stereoselectivity of radical mediated reductive alkylation of acyclic enamines
|Published in||Synlett. 1992, no. 3, p. 211-213|
|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|
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|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 https://archive-ouverte.unige.ch/unige:9968|