Source of Selectivity in Oxidative Cross‐Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol

E-ISSN： 1521-3765|21|35|12321-12325

ISSN： 0947-6539

Source： CHEMISTRY - A EUROPEAN JOURNAL, Vol.21, Iss.35, 2015-08, pp. : 12321-12325

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

Cover Picture: Source of Selectivity in Oxidative Cross‐Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol (Chem. Eur. J. 35/2015)

CHEMISTRY - A EUROPEAN JOURNAL, Vol. 21, Iss. 35, 2015-08 ,pp. : 12205-12205

John Wiley & Sons Inc

Access to resources Recommend Favorite

Significant Enhancement in the Efficiency and Selectivity of Iron‐Catalyzed Oxidative Cross‐Coupling of Phenols by Fluoroalcohols

ANGEWANDTE CHEMIE, Vol. 127, Iss. 14, 2015-03 ,pp. : 4272-4276

John Wiley & Sons Inc

Access to resources Recommend Favorite

Significant Enhancement in the Efficiency and Selectivity of Iron‐Catalyzed Oxidative Cross‐Coupling of Phenols by Fluoroalcohols

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 14, 2015-03 ,pp. : 4198-4202

John Wiley & Sons Inc

Access to resources Recommend Favorite

Copper‐Catalyzed Asymmetric Oxidative Cross‐Coupling of 2‐Naphthols with Aryl Methyl Ketones

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Vol. 2015, Iss. 7, 2015-03 ,pp. : 1569-1574

John Wiley & Sons Inc

Access to resources Recommend Favorite

Nickel Catalysis Enables Oxidative C(sp²)–H/C(sp²)–H Cross‐Coupling Reactions between Two Heteroarenes

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 55, Iss. 40, 2016-09 ,pp. : 12275-12279

John Wiley & Sons Inc

Access to resources Recommend Favorite