作者:Jie Chen、Xiao-Gang Fu、Ling Zhou、Jun-Tao Zhang、Xian-Liang Qi、Xiao-Ping Cao
DOI:10.1021/jo9003103
日期:2009.6.5
synthetic route to a class of marine natural products—malyngamides O (1), P (2), Q (3), R (4), 5′′-epi-3 and 5′′-epi-4—bearing a novel vinyl chloride structural motif was developed. The key steps involved construction of the vinyl chloride functionality by Wittig reaction, a DCC/HOBt-promoted amidation, an aldol reaction in the construction of the basic backbone of 1, 2, 3, 4, 5′′-epi-3, and 5′′-epi-4
一种收敛,对映选择性和通用的合成途径,可用于一类海洋天然产物-麦芽酰胺O(1),P(2),Q(3),R(4),5''- epi - 3和5''- epi - 4荷瘤的新型氯乙烯结构基序的开发。的关键步骤的通过维悌希反应中,DCC /添加HOBt促进的酰胺化,在基本骨架的结构的醛醇缩合反应的氯乙烯功能涉及建筑1,2,3,4,5'' -外延- 3,和5'' -外延-4,以及通过碱/酸条件或Mitsunobu反应使烯醇部分甲基化。此外,通过合成天然产物及其C-5''差向异构体,进一步证实了3中C-5''处的立体异构中心的绝对构型。