Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon

Convenient modification of the Leimgruber-Batcho indole synthesis: reduction of 2-nitro-β-pyrrolidinostyrenes by the FeCl3–activated carbon–N2H4∙H2O system

Published:2011-07 Issue:4 Volume:47 Page:425-434
ISSN:0009-3122
Container-title:Chemistry of Heterocyclic Compounds
language:en
Short-container-title:Chem Heterocycl Comp

Author:

Taydakov I. V.,Dutova T. Ya.,Sidorenko E. N.,Krasnoselsky S. S.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s10593-011-0776-2.pdf

Reference14 articles.

1. R. J. Sundberg, in: O. Meth-Cohn (editor), Best Synthetic Methods, Academic Press, London (1996), p. 7.

2. W. Leimgruber and A. D. Batcho, in: Third International Congress of Heterocyclic Chemistry, Japan, August 23–27, 1971, p. 462.

3. L. I. Kruse, Heterocycles, 16, 1119 (1981).

4. W. Leimgruber and A. D. Batcho, in: R. L. Danheiser (editor), Organic Synthesis, John Wiley & Sons, New York, Coll. vol. 7, p. 34 (1990); [vol. 65 (1985), p. 214].

5. R. D. Clark and D. B. Repke, Heterocycles, 22, 1119 (1984).

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