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Inside back cover: highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents (Angew. Chem. Int. Ed. 14/2012)

Farid, Umar and Wirth, Thomas 2012. Inside back cover: highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents (Angew. Chem. Int. Ed. 14/2012). Angewandte Chemie - International Edition 51 (14) , p. 3491. 10.1002/anie.201201230

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Abstract

About 30 % of the world's iodine production comes from the Chiba area in Japan, shown in the background of the picture (Map data ©2012 ZENRIN Imagery ©2012 TerraMetrics). Enantiomerically pure hypervalent iodine compounds are the key for metal-free, highly stereoselective oxyaminations of alkenes. In their Communication on page 3462 ff., T. Wirth and U. Farid report the use of the reaction for the facile synthesis of 2-arylprolinols.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: amino alcohols;aminohydroxylation;cyclization;hypervalent iodine;stereoselective synthesis
Publisher: Wiley-Blackwell
ISSN: 1433-7851
Last Modified: 04 Jun 2017 03:49
URI: http://orca-mwe.cf.ac.uk/id/eprint/27312

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