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

Farid, Umar and Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667 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:	20 Oct 2022 08:07
URI:	https://orca.cardiff.ac.uk/id/eprint/27312

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