Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/1181
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dc.contributor.authorKing’ondu, Cecil K.-
dc.contributor.authorKona, Jagadeswara R.-
dc.contributor.authorHowell, Amy R.-
dc.contributor.authorSuib, Steven L.-
dc.date.accessioned2015-04-17T08:18:16Z-
dc.date.available2015-04-17T08:18:16Z-
dc.date.issued2014-03-
dc.identifier.citationChemCatChem Volume 6, Issue 3, pages 749–752, March 2014en_US
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/cctc.201300942/abstract;jsessionid=B409C077C4F1A5119E6238283F92E468.f03t01?deniedAccessCustomisedMessage=&userIsAuthenticated=false-
dc.identifier.urihttp://repository.seku.ac.ke/handle/123456789/1181-
dc.descriptionDOI: 10.1002/cctc.201300942en_US
dc.description.abstractManganese 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.isoenen_US
dc.publisherWileyen_US
dc.subjectalcoholsen_US
dc.subjectheterogeneous catalysisen_US
dc.subjectmanganese oxideen_US
dc.subjectylidesen_US
dc.subjectunsaturated estersen_US
dc.titleOMS-2 for aerobic, catalytic, one-pot alcohol oxidation-wittig reactions: efficient access to α,β-unsaturated estersen_US
dc.typeArticleen_US
Appears in Collections:School of Science and Computing (JA)

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