Matsuda–Heck reaction with arenediazonium tosylates in water; Beilstein Journal of Organic Chemistry; Vol. 11

Matsuda–Heck reaction with arenediazonium tosylates in water

Dettagli Bibliografici
Parent link:	Beilstein Journal of Organic Chemistry.— , 20015- Vol. 11.— 2015.— [P. 358-362]
Enti autori:	Национальный исследовательский Томский политехнический университет (ТПУ) Институт физики высоких технологий (ИФВТ) Кафедра биотехнологии и органической химии (БИОХ), Национальный исследовательский Томский политехнический университет (ТПУ) Институт физики высоких технологий (ИФВТ) Кафедра общей и неорганической химии (ОНХ)
Altri autori:	Kutonova K. V. Ksenia Valentinovna, Trusova M. E. Marina Evgenievna, Stankevich A. V. Andrey Vladimirovich, Postnikov P. S. Pavel Sergeevich, Filimonov V. D. Viktor Dmitrievich
Riassunto:	Title screen An environmentally friendly Matsuda–Heck reaction with arenediazonium tosylates has been developed for the first time. A range of alkenes was arylated in good to quantitative yields in water. The reaction is significantly accelerated when carried out under microwave heating. The arylation of haloalkylacrylates with diazonium salts has been implemented for the first time.
Lingua:	inglese
Pubblicazione:	2015
Soggetti:	электронный ресурс труды учёных ТПУ циннаматы диазониевые соли стильбен alkyl cinnamates diazonium salts Matsuda–Heck reaction microwave-assisted synthesis stilbenes
Accesso online:	http://dx.doi.org/10.3762/bjoc.11.4
Natura:	Elettronico Capitolo di libro
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656634

Accesso online

http://dx.doi.org/10.3762/bjoc.11.4