| 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 |