Computing and Library Services - delivering an inspiring information environment

Chiral Aryl Iodide-Catalyzed Enantioselective α-Oxidation of Ketones

Rodríguez, Arantxa and Moran, Wesley J. (2012) Chiral Aryl Iodide-Catalyzed Enantioselective α-Oxidation of Ketones. Synthesis, 44 (8). pp. 1178-1182. ISSN 00397881

Metadata only available from this repository.


Several chiral aryl iodides were synthesized and assessed as catalysts in the enantioselective α-oxytosylation of propiophenone and the oxidative cyclization of 5-oxo-5-phenylpentanoic acid to 5-benzoyldihydrofuran-2(3H)-one. The highest enantioselectivities obtained were 18 and 51% ee, respectively. The latter is the highest selectivity recorded to date for this reaction.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Schools: School of Applied Sciences
Related URLs:
Depositing User: Sara Taylor
Date Deposited: 17 Apr 2012 15:17
Last Modified: 26 Jun 2012 10:07


Downloads per month over past year

Repository Staff Only: item control page

View Item View Item

University of Huddersfield, Queensgate, Huddersfield, HD1 3DH Copyright and Disclaimer All rights reserved ©