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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/1129


    Title: An efficacious synthetic strategy for cis-clerodane diterpenoids. Application to the total synthesis of (+/-)-6 beta-acetoxy-2-oxokolavenool
    Authors: Liu, HJ;Ho, YL;Wu, JD;Shia, KS
    Contributors: Division of Biotechnology and Pharmaceutical Research
    Abstract: An efficient synthetic strategy for cis-clerodane diterpenoids has been developed. The key ingredient is the face selective Diels-Alder reaction of dienophile 8. The successful application of this strategy has culminated in the total synthesis of the naturally occurring compound 6 beta -acetoxy-2-oxokolavenool in racemic form.
    Keywords: Chemistry, Organic
    Date: 2001-11
    Relation: Synlett. 2001 Nov(11):1805-1807.
    Link to: http://dx.doi.org/10.1055/s-2001-18105
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0936-5214&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000172040300035
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0034751735
    Appears in Collections:[夏克山] 期刊論文

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