Journal of the Chemical Society. Chemical communications p. 1105 - 1107 (1992)
Update date:2022-08-05
Topics:
Noiret, Nicolas
Youssofi, Abdullah
Carboni, Bertrand
Vaultier, Michel
Vinyldichloroboranes react with 1,3-dienes and the sequence Diels-Alder cycloaddition-reductive alkylation of benzyl azide leads directly to secondary amines, therefore, showing that vinyldichloroboranes behave as synthetic equivalents of secondary enamines of defined stereochemistry.
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(1992)
