Natural Products and Bioprospecting    2013, Vol. 3 Issue (6) : 288-294     DOI: 10.1007/s13659-013-0080-1
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Total synthesis and determination of the absolute configuration of a natural analgesic: crotonine
Yang YANGa,b
a State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
b Graduate University of Chinese Academy of Sciences, Beijing 100049, China
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Abstract  We report the first total synthesis of four possible absolute configurations and four other regional isomers of a naturally occurring alkaloid crotonine, which was isolated from Croton tiglium L. (Euphoriaceae) without elucidation of its absolute configuration. The concise five-step route with a chirally poor and regioselective strategy starting from monosaccharides was established, and the absolute structure of the natural crotonine was determined by comparison of the NMR spectra and optical rotations of the synthetic products.
Keywords total synthesis      crotonine      2-(furan-2-yl)-5-(2,3,4-trihydroxy-butyl)-1,4-diazine      Croton tiglium L. (Euphoriaceae)      analgesics     
Issue Date: 11 February 2018
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Yang YANG. Total synthesis and determination of the absolute configuration of a natural analgesic: crotonine[J]. Natural Products and Bioprospecting, 2013, 3(6): 288-294.
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http://npb.kib.ac.cn/EN/10.1007/s13659-013-0080-1     OR     http://npb.kib.ac.cn/EN/Y2013/V3/I6/288
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