Synthesis and transformations of 4-hydroxy-5-methyl-2-trifluoromethylpyridine-Reference-Cited by-同舟云学术

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Synthesis and transformations of 4-hydroxy-5-methyl-2-trifluoromethylpyridine

Published:1998-06 Issue:6 Volume:34 Page:679-682
ISSN:0009-3122
Container-title:Chemistry of Heterocyclic Compounds
language:en
Short-container-title:Chem Heterocycl Compd

Author:

Tyvorskii V. I.,Bobrov D. N.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Link

http://link.springer.com/content/pdf/10.1007/BF02252275.pdf

Reference15 articles.

1. M. A. McClinton and D. A. McClinton, Tetrahedron,48, 6555, 1992.

2. G. G. Furin, Zh. Org. Khim.,30, 1704 (1994).

3. M. J. Silvester, Aldrichim. Acta,24, 31 (1991).

4. EP Pat. 353187, H. G. Bruner; Chem. Abs.,113, 40462 (1990).

5. S. Adam, Tetrahedron,45, 1409 (1989).

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1. 2-(Trifluoromethyl)-4H-pyran-4-ones: Convenient, available and versatile building-blocks for regioselective syntheses of trifluoromethylated organic compounds;Journal of Fluorine Chemistry;2015-04

2. Fluorinated Pyrones, Chromones and Coumarins;Fluorine in Heterocyclic Chemistry Volume 2;2014

3. Reactions of 6-(tri- and 6-(difluoromethyl))comanic acids and their ethyl esters with aniline and its 2-substituted derivatives;Journal of Fluorine Chemistry;2012-09

4. 2-Cyano-6-(trifluoromethyl)-4H-pyran-4-one: A novel versatile CF3-containing building block;Journal of Fluorine Chemistry;2012-05

5. Facile synthesis of caerulomycin E by the formation of 2,2′-bipyridine core via a 2-pyridyl substituted 4H-pyran-4-one. Formal synthesis of caerulomycin A;Tetrahedron;2010-07

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