New trifluoromethylated sesquiterpenoids: synthesis, rearrangement, and biological activity-Reference-Cited by-同舟云学术

New trifluoromethylated sesquiterpenoids: synthesis, rearrangement, and biological activity

Published:2022 Issue:48 Volume:46 Page:23165-23172
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Gyrdymova Yulia V.¹^ORCID,Rumyantcev Roman V.²^ORCID,Esaulkova Yana L.³,Belyaevskaya Svetlana V.³,Zarubaev Vladimir V.³^ORCID,Kayumov Airat R.⁴^ORCID,Rubtsova Svetlana A.¹^ORCID

Affiliation:

1. Laboratory of Medicinal Chemistry, Institute of Chemistry, Ural Branch of the Russian Academy of Sciences, Syktyvkar, 167000, Russia

2. G. A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences, Nizhny Novgorod, 603950, Russia

3. Pasteur Institute of Epidemiology and Microbiology, St. Petersburg, 197101, Russia

4. Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia

Abstract

The tandem isomerization and trifluoromethylation reactions are a simple, convenient, and atom-economical strategy for the synthesis of various products in high yields from simple substrates.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ04611C

Reference54 articles.

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