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|Title:||A divergent approach to apoptolidin and FD-891: Asymmetric preparation of a common intermediate||Authors:||Chng, S.-S.
|Issue Date:||30-Jun-2003||Citation:||Chng, 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||Abstract:||Biologically 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.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/75408||ISSN:||00404039||DOI:||10.1016/S0040-4039(03)01173-0|
|Appears in Collections:||Staff Publications|
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