The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction; New Journal of Chemistry; Vol. 40, iss. 10

The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction

Bibliographic Details
Parent link:New Journal of Chemistry
Vol. 40, iss. 10.— 2016.— [P. 8855-8862]
Corporate Author: Национальный исследовательский Томский политехнический университет Институт физики высоких технологий Кафедра биотехнологии и органической химии
Other Authors: Khodja W. Walid, Leclair A. Alexandre, Rull-Barrull J. Jordi, Zammattio F. Francoise, Kutonova K. V. Ksenia Valentinovna, Trusova M. E. Marina Evgenievna, Felpin F.-Х. Francois-Xavier, Rodriguez Z. M. Zubiri Mireia
Summary:Title screen
An efficient Pd-catalyzed arylation reaction of challenging acyclic olefins, in the presence of an organic ligand, has been disclosed. Commercially available cheap pyridine-based ligands are able to promote good to excellent yields for poorly efficient Heck–Matsuda arylation reactions of several allylic alcohols. A wide range of electronically different arenediazonium salts bearing either electron-releasing or withdrawing groups have been used allowing the synthesis of a range of Я-aryl-methoxy-lactols. The catalytic system has been optimised, along with the reaction conditions, in order to achieve remarkable yields in less than 1 h.
Режим доступа: по договору с организацией-держателем ресурса
Language:English
Published: 2016
Subjects:
электронный ресурс
труды учёных ТПУ
Online Access:http://dx.doi.org/10.1039/C6NJ01717G
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=650629

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