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

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
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

Internet

http://dx.doi.org/10.1039/C6NJ01717G