Trifluoromethyl group in the synthesis of heterocyclic compounds: New and efficient synthesis of 3-aryl-4-aminocinnolines-Reference-Cited by-同舟云学术

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Trifluoromethyl group in the synthesis of heterocyclic compounds: New and efficient synthesis of 3-aryl-4-aminocinnolines

Published:1995-02 Issue:9 Volume:36 Page:1383-1386
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kiselyov Alexander S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Tetrahedron report number 221

2. Filler, R.; Kobayashi, Y., Eds.; Kodansha Ltd. & Elsevier Biomedical: Tokyo, Amsterdam, New York, Oxford 1982.

3. Chemistry of Organic Fluorine Compounds;Hudlicky,1992

4. Introduction of fluorine into organic molecules: why and how

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1. Anion-Driven C–F Bond Activation of Trifluoromethyl N-Aryl Hydrazones: Application to the Synthesis of 1,3,4-Oxadiazoles;The Journal of Organic Chemistry;2023-10-20

2. Divergent synthesis of fused N-heterocycles via rhodium-catalysed [4 + 2] cyclization of pyrazolidinones with iodonium ylides;Organic Chemistry Frontiers;2022

3. Copper-Catalyzed Cascade Cyclization of Arylsulfonylhydrazones Derived from ortho-Alkynyl Arylketones: Regioselective Synthesis of Functionalized Cinnolines;Organic Letters;2019-11-11

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