Reaction of methyl esters of substituted 2-oxochromene-3-carboxylic acids with zinc enolates formed from 1-aryl-2-bromoalkanones-Reference-Cited by-同舟云学术

Reaction of methyl esters of substituted 2-oxochromene-3-carboxylic acids with zinc enolates formed from 1-aryl-2-bromoalkanones

Published:2004-09 Issue:9 Volume:74 Page:1410-1413
ISSN:1070-3632
Container-title:Russian Journal of General Chemistry
language:en
Short-container-title:Russ J Gen Chem

Author:

Shchepin V. V.,Korzun A. E.,Shurov S. N.,Vakhrin M. I.,Russkikh N. Yu.

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s11176-005-0022-7.pdf

Reference4 articles.

1. Shchepin, V.V., Kalyuzhnyi, M.M., and Shchepin, R.V., Khim. Geterotsikl. Soedin., 2001, no. 10, p. 1415.

2. Stewart, J.J.P., J. Comput. Chem., 1989, vol. 10, no.2, p. 209.

3. Gordon, A.J. and Ford, R.A., The Chemist’s Companion, New York: Wiley, 1972. Translated under the title Sputnik khimika, Moscow: Mir, 1976, p. 297.

4. Stewart, J.J.P., Mopac 7.0, Frank J. Seilor Res. Lab. US Air Force Academy, QCPM 175.

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3. Reactions of zinc enolates derived from 1-aryl-2-bromo-2-phenylethanone and 2-bromoindan-1-one with alkyl 2-oxochromene-and 6-bromo-2-oxochromene-3-carboxylates;Russian Journal of General Chemistry;2006-05