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

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

Podrobná bibliografie
Parent link:	Beilstein Journal of Organic Chemistry.— , 20015- Vol. 11.— 2015.— [P. 358-362]
Korporace:	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)
Další autoři:	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
Shrnutí:	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.
Jazyk:	angličtina
Vydáno:	2015
Témata:	электронный ресурс труды учёных ТПУ циннаматы диазониевые соли стильбен alkyl cinnamates diazonium salts Matsuda–Heck reaction microwave-assisted synthesis stilbenes
On-line přístup:	http://dx.doi.org/10.3762/bjoc.11.4
Médium:	Elektronický zdroj Kapitola
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656634

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