OMS-2 for aerobic, catalytic, one-pot alcohol oxidation-wittig reactions: efficient access to α,β-unsaturated esters

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dc.contributor.author King’ondu, Cecil K.
dc.contributor.author Kona, Jagadeswara R.
dc.contributor.author Howell, Amy R.
dc.contributor.author Suib, Steven L.
dc.date.accessioned 2015-04-17T08:18:16Z
dc.date.available 2015-04-17T08:18:16Z
dc.date.issued 2014-03
dc.identifier.citation ChemCatChem Volume 6, Issue 3, pages 749–752, March 2014 en_US
dc.identifier.uri http://onlinelibrary.wiley.com/doi/10.1002/cctc.201300942/abstract;jsessionid=B409C077C4F1A5119E6238283F92E468.f03t01?deniedAccessCustomisedMessage=&userIsAuthenticated=false
dc.identifier.uri http://repository.seku.ac.ke/handle/123456789/1181
dc.description DOI: 10.1002/cctc.201300942 en_US
dc.description.abstract Manganese oxide octahedral molecular sieve (OMS) materials with well-defined pores have been extensively studied over two decades due to their intriguing chemical and physical properties. OMS-2, the synthetic cryptomelane form of manganese oxide, was synthesized by a modified reflux method and was found to be highly active for obtaining α,β-unsaturated esters (up to 95 % yield and with high diastereoselectivities) from a variety of benzyl, heteroaryl, allyl and alkyl alcohols via one-pot alcohol oxidation-Wittig reaction. The transformation utilizes air as the stoichiometric oxidant, and the inexpensive catalyst can be recovered and reused. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject alcohols en_US
dc.subject heterogeneous catalysis en_US
dc.subject manganese oxide en_US
dc.subject ylides en_US
dc.subject unsaturated esters en_US
dc.title OMS-2 for aerobic, catalytic, one-pot alcohol oxidation-wittig reactions: efficient access to α,β-unsaturated esters en_US
dc.type Article en_US


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