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Reductive amination in the synthesis of azaheterocycles (review)

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00546725· OSTI ID:6961643

Methods for obtaining saturated five- and six-membered azaheterocycles based on the use of catalytic intra- and intermolecular hydroamination of dicarbonyl compounds and ketones and amines of the furan series, hydride amination of aldehydes and ketones, and the Leuckart reaction are examined. The authors attempted to thoroughly analyze these reactions as a function of the structures of the starting substances, the character of the reducing agent, and the conditions of the processes and to correlate the literature data published in recent years.

Research Organization:
N. G. Chernyshevskii Saratov State Univ. (USSR)
OSTI ID:
6961643
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 23:4; ISSN CHCCA
Country of Publication:
United States
Language:
English