Catalyst-free 1 : 2 annulation of quinolines with trifluoroacetylacetylenes: an access to functionalized oxazinoquinolines-Reference-Cited by-同舟云学术

Catalyst-free 1 : 2 annulation of quinolines with trifluoroacetylacetylenes: an access to functionalized oxazinoquinolines

Published:2018 Issue:43 Volume:16 Page:8038-8041
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Belyaeva K. V.¹²³⁴,Nikitina L. P.¹²³⁴,Afonin A. V.¹²³⁴,Vashchenko A. V.¹²³⁴,Muzalevskiy V. M.⁵⁶⁷⁸,Nenajdenko V. G.⁵⁶⁷⁸^ORCID,Trofimov B. A.¹²³⁴^ORCID

Affiliation:

1. A. E. Favorsky Irkutsk Institute of Chemistry

2. Siberian Branch

3. Russian Academy of Sciences

4. Irkutsk

5. M. V. Lomonosov Moscow State University

6. Department of Chemistry

7. Moscow

8. 119991 Russian Federation

Abstract

Catalyst-free reaction of quinolines with two molecules of aryltrifluoroacetylacetylenes afforded 3-arylethynyl-3-trifluoromethyl-1,3-oxazinoquinolines in up to 92% yields.

Funder

Russian Foundation for Basic Research

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02379D

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