Diastereoselective heterocyclization of geminal bromo-fluoro arylcyclopropanes by nitrosonium tetrafluoroborate: Access to 4-fluorinated isoxazolines and isoxazoles-Reference-Cited by-同舟云学术

Diastereoselective heterocyclization of geminal bromo-fluoro arylcyclopropanes by nitrosonium tetrafluoroborate: Access to 4-fluorinated isoxazolines and isoxazoles

Published:2019-11 Issue:46 Volume:75 Page:130666
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bondarenko Oksana B.,Komarov Arseniy I.,Karetnikov George L.,Nikolaeva Svetlana N.,Zyk Nikolai V.,Holt Tina,Kutateladze Andrei G.

Funder

National Science Foundation

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Synthesis of 5-fluoro- and 5-bromoalkylisoxazoles via nitrosation of 1,1-dihalocyclopropanes with sulfur trioxide activated nitrosyl chloride

2. Access to 5-fluoroisoxazoles via the nitrosation of geminal bromo-fluoro arylcyclopropanes

3. Nitronium salts as novel reagents for the heterocyclization of gem-bromofluorocyclopropanes into pyrimidine derivatives

4. A novel and effective approach to 4-fluoropyrimidines

5. Nitrosation of 2-aryl-1-bromo-1-fluorocyclopropanes with nitrosonium tetrafluoroborate as an approach to the synthesis of 5-aryl-4-bromo-4-fluoroisoxazolines

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