BF3-ETHERATE PROMOTED ALKYLATION OF AZIRIDINES WITH ORGANOCOPPER REAGENTS: A NEW SYNTHESIS OF AMINES

DOI: 10.1016/S0040-4039(00)98420-X

Source and publish data:

Tetrahedron Letters p. 1153 - 1156 (1985)

Update date:2022-08-05

Topics:

Authors:

Eis, Michael J.

Ganem, Bruce

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Article abstract of DOI:10.1016/S0040-4039(00)98420-X

Boron trifluoride etherate promotes nucleophilic ring opening of a variety of substituted aziridines by diorganocopperlithium reagents leading to both primary and secondary amines.

Full text of DOI:10.1016/S0040-4039(00)98420-X

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