Nickel‐Catalyzed Mizoroki–Heck Reaction of Aryl Sulfonates and Chlorides with Electronically Unbiased Terminal Olefins: High Selectivity for Branched Products

Publisher： John Wiley & Sons Inc

E-ISSN： 1521-3773|53|7|1858-1861

ISSN： 1433-7851

Source： ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol.53, Iss.7, 2014-02, pp. : 1858-1861

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Nickel‐Catalyzed Mizoroki–Heck Reaction of Aryl Sulfonates and Chlorides with Electronically Unbiased Terminal Olefins: High Selectivity for Branched Products

By  

ANGEWANDTE CHEMIE, Vol. 126, Iss. 7, 2014-02 ,pp. : 1889-1892

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mizoroki–Heck Reaction of Aryl Halides and Dialkyl Allylphosphonates in Water Catalyzed by Reusable Palladium Nanoparticles

By  

ASIAN JOURNAL OF ORGANIC CHEMISTRY, Vol. 4, Iss. 10, 2015-10 ,pp. : 1112-1119

John Wiley & Sons Inc

Access to resources Recommend Favorite

Silver sequestration of halides for the activation of Pd(OAc)2 catalyzed Mizoroki‐Heck reaction of 1,1 and 1,2 ‐ Disubstituted alkenes

By  

APPLIED ORGANOMETALLIC CHEMISTRY (ELECTRONIC), Vol. 32, Iss. 3, 2018-03 ,pp. : n/a-n/a

John Wiley & Sons Inc

Access to resources Recommend Favorite

ChemInform Abstract: Skutterudites as Thermoelectric Materials: Revisited

By  

CHEMINFORM (ELECTRONIC), Vol. 46, Iss. 29, 2015-07 ,pp. : no-no

John Wiley & Sons Inc

Access to resources Recommend Favorite

Nickel‐Catalyzed Cross‐Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes

By  

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 53, Iss. 37, 2014-09 ,pp. : 9909-9913

John Wiley & Sons Inc

Access to resources Recommend Favorite