Synthesis of (2s,3r,4e,8e)-<math><mtext>n</mtext></math>-(2′r)-2′-hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine,the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete <math><mtext>schizophyllum</mtext></math><math><mtext>commune</mtext></math>期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Synthesis of (2s,3r,4e,8e)- $n$ -(2′r)-2′-hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine,the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete $schizophyllum$ $commune$

Authors:	Kenji Mori Yuji Funaki

Institution:	Department of Agricultural Chemistry, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113, Japan

Abstract:	A total synthesis of the natural enantiomer of the title compound was accomplished, which confirmed the structure proposed for the fruiting-inducing cerebroside of $Schizophyllum$ $commune$ .

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