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Highly enantioselective oxidation of aryl benzyl sulfides

Academic Article
Publication Date:
2011
abstract:
Enantiopure aryl benzyl sulfoxides were easily obtained by an enantioselective oxidation of the corresponding sulfides with tert-butyl hydroperoxide in the presence of a complex between titanium and (S, S)-or (R, R)-hydrobenzoin. Theoretical and experimental investigations confirmed that these aryl benzyl sulfides represent an ideal substrate for the asymmetric oxidation system. Copyright © Taylor and Francis Group, LLC.
Iris type:
01.01 Articolo in rivista
Keywords:
Hydrobenzoin; Oxidation mechanism; Sulfoxide; Titanium complex
List of contributors:
Naso, Francesco; Capozzi, MARIA ANNUNZIATA; Cardellicchio, Cosimo
Authors of the University:
CARDELLICCHIO COSIMO
Handle:
https://iris.cnr.it/handle/20.500.14243/147445
Published in:
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-79960518253&origin=inward
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