Tetrahedron Letters p. 627 - 630 (1992)
Update date:2022-08-29
Topics:
Itsuno, Shinichi
Hachisuka, Chiharu
Kitano, Keisuke
Ito, Koichi
The partial reduction of nitriles with several alkylboranes produced an addition product, N-boryl imine, which was readily converted to secondary carbinamine by treatment with organolithium or Grignard reagents. Optically active N-boryl imines were also prepared from chiral borane and nitrile for the chiral amine synthesis.
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