Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(03)01173-0
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dc.titleA divergent approach to apoptolidin and FD-891: Asymmetric preparation of a common intermediate
dc.contributor.authorChng, S.-S.
dc.contributor.authorXu, J.
dc.contributor.authorLoh, T.-P.
dc.date.accessioned2014-06-23T05:29:59Z
dc.date.available2014-06-23T05:29:59Z
dc.date.issued2003-06-30
dc.identifier.citationChng, S.-S., Xu, J., Loh, T.-P. (2003-06-30). A divergent approach to apoptolidin and FD-891: Asymmetric preparation of a common intermediate. Tetrahedron Letters 44 (27) : 4997-5000. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(03)01173-0
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75408
dc.description.abstractBiologically active Apoptolidin and FD-891 have structural similarity in their macrocyclic cores. Asymmetric preparation of a common intermediate in the total synthesis of these two macrolides is presented. A modified Masuyama Sn-allylation was employed to control the relative stereochemistry in the synthesis of the intermediate. © 2003 Elsevier Science Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0040-4039(03)01173-0
dc.sourceScopus
dc.subjectApoptolidin
dc.subjectDivergent synthesis
dc.subjectFD-891
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/S0040-4039(03)01173-0
dc.description.sourcetitleTetrahedron Letters
dc.description.volume44
dc.description.issue27
dc.description.page4997-5000
dc.description.codenTELEA
dc.identifier.isiut000183683500012
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