对原卫矛素的合成研究：呋喃基-环丁酮片段的高效构建
Synthetic Studies Toward Providencin: Efficient Construction of a Furanyl-Cyclobutanone Fragment.
作者信息
Stevens Sarah J, Bérubé Amélie, Wood John L
机构信息
Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
出版信息
Tetrahedron. 2011 Sep 2;67(35):6479-6481. doi: 10.1016/j.tet.2011.06.002.
Abstract
Described is the construction of a furanyl-cylcobutanone fragment suited for incorporation into a synthesis of the naturally occurring anti-cancer agent Providencin.
摘要
描述了一种呋喃基环丁酮片段的构建，该片段适合纳入天然抗癌剂普罗维登菌素的合成中。
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本文引用的文献
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Synthesis of the cyclobutylfuran sector of providencin via zirconium-mediated oxygen abstraction from a furanoside.通过锆介导的从呋喃糖苷中提取氧来合成普罗维登菌素的环丁基呋喃部分。
Org Lett. 2009 Mar 19;11(6):1433-6. doi: 10.1021/ol900152p.
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Exploring biosynthetic relationships among furanocembranoids: synthesis of (-)-bipinnatin J, (+)-intricarene, (+)-rubifolide, and (+)-isoepilophodione B.探索呋喃贝壳杉烷类化合物之间的生物合成关系：（-）-双羽状叶素J、（+）-内贝壳杉烯、（+）-红没药醇和（+）-异表叶蝉二酮B的合成
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Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogues.环丁基核苷类似物对映体形式的合成及抗病毒活性
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