Polyfluoroalkylated antipyrines in Pd-catalyzed transformations-Reference-Cited by-同舟云学术

Polyfluoroalkylated antipyrines in Pd-catalyzed transformations

Published:2021 Issue:56 Volume:11 Page:35174-35181
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Shchegolkov Evgeny V.¹^ORCID,Burgart Yanina V.¹^ORCID,Matsneva Daria A.¹,Borisevich Sophia S.²,Kadyrova Renata A.³,Orshanskaya Iana R.³,Zarubaev Vladimir V.³^ORCID,Saloutin Victor I.¹^ORCID

Affiliation:

1. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, S. Kovalevskoi St., 22, Ekaterinburg 620990, Russia

2. Ufa Institute of Chemistry, Russian Academy of Sciences, 71 October Ave., Ufa, 450054, Russia

3. Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology, 14 Mira St., Saint-Petersburg, 197101, Russia

Abstract

Peculiarities of heterocyclic systems with electron-withdrawing groups (polyfluoroalkyl-containing antipyrines) in Pd-catalyzed C–H arylation and cross-coupling reactions.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA06967E

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1. Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities

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