

Publisher: John Wiley & Sons Inc
E-ISSN: 1521-3757|127|27|7968-7972
ISSN: 0044-8249
Source: ANGEWANDTE CHEMIE, Vol.127, Iss.27, 2015-06, pp. : 7968-7972
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
AbstractA novel method for the synthesis of a wide range of functionalized 1,3‐diol derivatives is reported. Employing a copper‐catalyzed oxy‐alkenylation strategy, a range of readily available, substituted homoallylic alcohol derivatives and alkenyl(aryl) iodonium salts combine to form syn‐1,3‐carbonates in excellent yield and with high selectivity. Furthermore, the products formed are amenable to an iterative reaction sequence, thus affording highly complex polyketide‐like fragments.
Related content






A TEMPO‐Free Copper‐Catalyzed Aerobic Oxidation of Alcohols
ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 14, 2015-03 ,pp. :


A TEMPO‐Free Copper‐Catalyzed Aerobic Oxidation of Alcohols
ANGEWANDTE CHEMIE, Vol. 127, Iss. 14, 2015-03 ,pp. :


Copper‐Catalyzed Dehydrogenative Coupling of Arenes with Alcohols
ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 52, Iss. 35, 2013-08 ,pp. :