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Convenient synthesis of symmetrical diketosulfides from enolizable ketones using [hydroxy(tosyloxy)iodo]benzene and na2S ⋅ 9H2O

Convenient synthesis of symmetrical diketosulfides from enolizable ketones using... An efficient method for the preparation of symmetrical diketosulfides of the type ArCOCH2SCH2COAr has been developed from the reaction of [hydroxy(tosyloxy)iodo]benzene with various acetophenones, followed by treatment with Na2S ⋅ 9H2O. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:172–176, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20524 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Convenient synthesis of symmetrical diketosulfides from enolizable ketones using [hydroxy(tosyloxy)iodo]benzene and na2S ⋅ 9H2O

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References (29)

Publisher
Wiley
Copyright
Copyright © 2009 Wiley Subscription Services
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.20524
Publisher site
See Article on Publisher Site

Abstract

An efficient method for the preparation of symmetrical diketosulfides of the type ArCOCH2SCH2COAr has been developed from the reaction of [hydroxy(tosyloxy)iodo]benzene with various acetophenones, followed by treatment with Na2S ⋅ 9H2O. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:172–176, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20524

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 2009

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