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Chemo- and regioselective hydroboration of Δ^(14,15) in certain cephalostatin analogue
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作者 mansour nawasreh 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第12期1391-1394,共4页
The symmetrical diketone Ⅱ, which can be synthesized in gram scale using a well established method, was used as a starting material to prepare the 11α-methoxy ketomethylene Ⅵ. This is in continuation of our study a... The symmetrical diketone Ⅱ, which can be synthesized in gram scale using a well established method, was used as a starting material to prepare the 11α-methoxy ketomethylene Ⅵ. This is in continuation of our study aiming at the synthesis of multihydroxylated cephalostatin analogues, as for example cephalostatin 1Ⅰ, a potent anti-tumor natural product. Compound Ⅵ underwent chemo- and regioselective hydroboration reaction at only one of △14.15 double bonds furnishing compound Ⅸ as a major product in a fair yield. 展开更多
关键词 Cephalostatin 1 DIKETONE Hydroboration of △^14 15 double bond Anti-cancer activity
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