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dc.contributor.authorVenukadasula, Phanindra K. M.
dc.contributor.authorChegondi, Rambabu
dc.contributor.authorMaitra, Soma
dc.contributor.authorHanson, Paul R.
dc.date.accessioned2017-03-08T19:08:10Z
dc.date.available2017-03-08T19:08:10Z
dc.date.issued2010-04
dc.identifier.citationVenukadasula, P. K. M., Chegondi, R., Maitra, S., & Hanson, P. R. (2010). A Concise, Phosphate-Mediated Approach to the Total Synthesis of (−)-Tetrahydrolipstatin. Organic Letters, 12(7), 1556–1559. http://doi.org/10.1021/ol1002913en_US
dc.identifier.urihttp://hdl.handle.net/1808/23359
dc.description.abstractAn efficient synthesis of (−)-tetrahydrolipstatin (THL) is reported. This method takes advantage of a phosphate tether-mediated, one-pot, sequential RCM/CM/hydrogenation protocol to deliver THL in 8 total steps from a readily prepared (S,S)-triene. The strategy incorporates selective cross metathesis, regio-selective hydrogenation, regio- and diastereoselective cuprate addition and Mitsunobu inversion for installation of the C5 formamide ester subunit.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/ol1002913en_US
dc.titleA Concise, Phosphate-Mediated Approach to the Total Synthesis of (−)-Tetrahydrolipstatinen_US
dc.typeArticleen_US
kusw.kuauthorVenukadasula, Phanindra K. M.
kusw.kuauthorChegondi, Rambabu
kusw.kuauthorMaitra, Soma
kusw.kuauthorHanson, Paul R.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1021/ol1002913en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccess


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