Preparation of secondary carbinamines via alkylation of N-boryl imines generated from partial reduction of nitriles with NABH4-carboxylic acid

Article abstract of DOI:10.1080/00397919208021137

Secondary carbinamines have been prepared from alkylation of N-boryl imines which were generated in situ from partial reduction of nitriles with sodium borohydride modified by carboxylic acid.

Full text of DOI:10.1080/00397919208021137

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Preparation of Secondary
Carbinamines via Alkylation of
N-Boryl Imines Generated from
Partial Reduction of Nitriles
with NABH4-Carboxylic Acid
Shinichi Itsuno a , Chiharu Hachisuka a , Yoshiko
Ushijima a & Koichi Ito a
a Department of Materials Science, Toyohashi
University of Technology Tempaku-cho, Toyohashi,
441, Japan
Available online: 23 Sep 2006
To cite this article: Shinichi Itsuno, Chiharu Hachisuka, Yoshiko Ushijima & Koichi
Ito (1992): Preparation of Secondary Carbinamines via Alkylation of N-Boryl Imines
Generated from Partial Reduction of Nitriles with NABH4-Carboxylic Acid, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:22, 3229-3234
To link to this article: http://dx.doi.org/10.1080/00397919208021137
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