首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Enantioselective total synthesis of polyoxygenated cyclohexanoids:(+)-streptol,ent-RKTS-33 and putative '(+)-parasitenone'.Identity of parasitenone with (+)-epoxydon
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Enantioselective total synthesis of polyoxygenated cyclohexanoids:(+)-streptol,ent-RKTS-33 and putative '(+)-parasitenone'.Identity of parasitenone with (+)-epoxydon

机译:(+)-链烷醇,ent-RKTS-33和推定的'(+)-parasitenone'的对映选择性全合成。(+)-环氧的对位寄生虫的身份

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摘要

Short,simple and enantioselective syntheses of the natural product (+)-streptol,the non-peptide apoptosis inhibitor ent-RKTS-33 and the putative structure of 'parasitenone' have been accomplished from the readily available chiral building block.'Parasitenone' has been shown to be identical with the known natural product epoxydon.
机译:天然产物(+)-链烷醇,非肽凋亡抑制剂ent-RKTS-33的短,简单和对映选择性合成是通过容易获得的手性结构单元完成的。已证明与已知的天然产物环氧龙胆相同。

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