Matsuda–Heck reaction with arenediazonium tosylates in water

Matsuda–Heck reaction with arenediazonium tosylates in water

מידע ביבליוגרפי
Parent link:Beilstein Journal of Organic Chemistry.— , 20015-
Vol. 11.— 2015.— [P. 358-362]
Corporate Authors: 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)
מחברים אחרים: 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
סיכום: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.
שפה:אנגלית
יצא לאור: 2015
נושאים:
электронный ресурс
труды учёных ТПУ
циннаматы
диазониевые соли
стильбен
alkyl cinnamates
diazonium salts
Matsuda–Heck reaction
microwave-assisted synthesis
stilbenes
גישה מקוונת:http://dx.doi.org/10.3762/bjoc.11.4
פורמט: אלקטרוני Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656634
תיאור
סיכום: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.
DOI:10.3762/bjoc.11.4

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