Issue 7, 1991

Preparation of secondary carbinamines via N-boryl imines generated in situ from nitriles and borane–tetrahydrofuran

Abstract

N-Boryl imines obtained from partial reduction of nitriles with borane–tetrahydrofuran have been alkylated with organolithium or Grignard reagents to afford secondary carbinamines in moderate to excellent yields.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 1767-1769

Preparation of secondary carbinamines via N-boryl imines generated in situ from nitriles and borane–tetrahydrofuran

S. Itsuno, C. Hachisuka and K. Ito, J. Chem. Soc., Perkin Trans. 1, 1991, 1767 DOI: 10.1039/P19910001767

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