Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/93671
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dc.titleEfficient construction of the kedarcidin chromophore ansamacrolide
dc.contributor.authorKoyama, Y.
dc.contributor.authorLear, M.J.
dc.contributor.authorYoshimura, F.
dc.contributor.authorOhashi, I.
dc.contributor.authorMashimo, T.
dc.contributor.authorHirama, M.
dc.date.accessioned2014-10-16T08:27:01Z
dc.date.available2014-10-16T08:27:01Z
dc.date.issued2005-01-20
dc.identifier.citationKoyama, Y.,Lear, M.J.,Yoshimura, F.,Ohashi, I.,Mashimo, T.,Hirama, M. (2005-01-20). Efficient construction of the kedarcidin chromophore ansamacrolide. Organic Letters 7 (2) : 267-270. ScholarBank@NUS Repository.
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93671
dc.description.abstract(Chemical Equation Presented) The streamlined assembly of the ansamacrolide framework of the kedarcidin chromophore via an efficient atropselective Sonogashira coupling step is described. To this end, two newly improved practical syntheses of the cyclopentene and diyne fragments have been developed, which feature 0.2 mol % catalytic loadings for an RCM step and i-PrMgCl/CH 2I2 as a new entry to gem-disubstituted epoxides from ketones, both being applicable to 49-g scales.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleOrganic Letters
dc.description.volume7
dc.description.issue2
dc.description.page267-270
dc.identifier.isiutNOT_IN_WOS
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