Ultra-fast Suzuki and Heck reactions for the synthesis of styrenes and stilbenes using arenediazonium salts as super-electrophiles; Organic Chemistry Frontiers; Vol. 5, iss. 1

Bibliografische gegevens
Parent link:Organic Chemistry Frontiers
Vol. 5, iss. 1.— 2018.— [P. 41-45]
Coauteur: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Andere auteurs: Trusova M. E. Marina Evgenievna, Rodriguez-Zubiri M. Mireia, Kutonova K. V. Ksenia, Jung N. Nicole, Brase S. Stefan, Francois-Xavier F. Felpin, Postnikov P. S. Pavel Sergeevich
Samenvatting:Title screen
The super-electrophilic properties of arenediazonium salts have been exploited for achieving ultra-fast palladium-catalyzed coupling reactions with turnover frequencies up to 16 200 h−1. These ultra-fast coupling reactions have been exemplified with the synthesis of prone-to-polymerization styrenes within seconds through Suzuki cross-couplings with potassium vinyltrifluoroborate. Heterocycles and functional groups such as halides were well tolerated. The ambivalent properties of potassium vinyltrifluoroborate also allowed the development of ultra-fast sequential Suzuki-Heck reactions for the preparation of symmetrical and unsymmetrical stilbenes within minutes.
Режим доступа: по договору с организацией-держателем ресурса
Taal:Engels
Gepubliceerd in: 2018
Onderwerpen:
Online toegang:https://doi.org/10.1039/C7QO00750G
Formaat: Elektronisch Hoofdstuk
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667206

MARC

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200 1 |a Ultra-fast Suzuki and Heck reactions for the synthesis of styrenes and stilbenes using arenediazonium salts as super-electrophiles  |f M. E. Trusova, M. Rodriguez-Zubiri, K. V. Kutonova [et al.] 
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330 |a The super-electrophilic properties of arenediazonium salts have been exploited for achieving ultra-fast palladium-catalyzed coupling reactions with turnover frequencies up to 16 200 h−1. These ultra-fast coupling reactions have been exemplified with the synthesis of prone-to-polymerization styrenes within seconds through Suzuki cross-couplings with potassium vinyltrifluoroborate. Heterocycles and functional groups such as halides were well tolerated. The ambivalent properties of potassium vinyltrifluoroborate also allowed the development of ultra-fast sequential Suzuki-Heck reactions for the preparation of symmetrical and unsymmetrical stilbenes within minutes. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Organic Chemistry Frontiers 
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701 1 |a Francois-Xavier  |b F.  |g Felpin 
701 1 |a Postnikov  |b P. S.  |c organic chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of chemical sciences  |f 1984-  |g Pavel Sergeevich  |3 (RuTPU)RU\TPU\pers\31287  |9 15465 
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