Lower primary alkanols and their esters in a Ritter-type reaction with nitriles. An efficient method for obtaining N-primary-alkyl amides-Reference-Cited by-同舟云学术

Lower primary alkanols and their esters in a Ritter-type reaction with nitriles. An efficient method for obtaining N-primary-alkyl amides

Published:2002-02 Issue:8 Volume:43 Page:1397-1399
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Lebedev Mikhail Y.,Erman Mark B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. For reviews on the Ritter reaction, see: (a) Krimen, L. I.; Cota, D. J. In Organic Reactions; Dauben, W. G., Ed.; John Wiley & Sons: New York, 1969; Vol. 17; pp. 213–325; (b) Bishop, R. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I.; Eds.; Pergamon Press: New York, 1991; Vol. 6, pp. 261–300.

2. A New Reaction of Nitriles. I. Amides from Alkenes and Mononitriles1

3. A New Reaction of Nitriles. III. Amides from Dinitriles

4. N-Alkylation of Nitriles with Benzyl Alcohol, Related Alcohols, and Glycols1

5. Amides from Nitriles and Alcohols by the Ritter Reaction

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