CAS: 23708-48-7; Bromo-[5-(Bromomagnesio)Pentyl]Magnesium

该化合物是一种二基甘醇试剂,在两个镁中心(每个中心都与溴原子捆绑在一起)之间有一个五甲基桥梁,这一结构增强了其在交叉和核分裂生殖反应中的回活动性,特别是在循环或延长有机框架合成中.硬性1,5-五溴二苯醚二酰氟航天器提供了稳定性,同时保持了高度的功能性群体耐受性.它对于编制大型循环化合物和聚合物前体,提供受控的蒸气测量和减少侧面反应,特别有用.由于对空气和湿度的敏感性,该试剂通常在惰性条件下处理.其多功能性使得其在有机金属和材料化学研究中具有价值.

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    专利信息


    专利号:US-8258362-B2
    优先权日:2009-05-04
    标 题:Method for the production of α, ω-olefins by using the copper catalyzed coupling reaction of a Grignard reagent with an allylic substrate
    发明人:NACHARAJU KRISHNAMURTHY; TAYLOR PAUL D; COONEY MARK J; CRABTREE LARRY A
    权利人:NACHARAJU KRISHNAMURTHY; TAYLOR PAUL D; COONEY MARK J; CRABTREE LARRY A; ISP INVESTMENTS INC
    摘要:A process for the synthesis of linear α,ω-diolefins from an allylic substrate comprises the steps of a) forming the bis-Grignard reagent XMgCH2(CH2)nCH2MgX from an α,ω-acyclic dihalide with X being a halogen; b) preparing a solution comprising an allylic substrate and a copper catalyst; c) catalyzing a coupling reaction by adding to the solution of step (b) the bis-Grignard reagent of step (a); and d) isolating and purifying the α,ω-olefin coupling reaction product.

    专利号:US-8487108-B2
    优先权日:2005-11-14
    标题 :Piperidinyl carbamate intermediates for the synthesis of aspartic protease inhibitors
    发明人:BALDWIN JOHN J; CLAREMON DAVID A; TICE COLIN; CACATIAN SALVACION; DILLARD LAWRENCE W; ISHCHENKO ALEXEY V; YUAN JING; XU ZHENRONG; MCGEEHAN GERARD; SIMPSON ROBERT D; SINGH SURESH B; ZHAO WEI; FLAHERTY PATRICK T
    权利人:BALDWIN JOHN J; CLAREMON DAVID A; TICE COLIN; CACATIAN SALVACION; DILLARD LAWRENCE W; ISHCHENKO ALEXEY V; YUAN JING; XU ZHENRONG; MCGEEHAN GERARD; SIMPSON ROBERT D; SINGH SURESH B; ZHAO WEI; FLAHERTY PATRICK T; VITAE PHARMACEUTICALS INC
    摘要:The present invention is directed to aspartic protease inhibitors. Certain aspartic protease inhibitors of the invention can be represented by the following structural formula or a pharmaceutically acceptable salt thereof. The present invention is also directed to pharmaceutical compositions comprising the disclosed aspartic protease inhibitors. The present invention is further directed to methods of antagonizing one or more aspartic proteases in a subject in need thereof, and methods for treating an aspartic protease mediated disorder in a subject using the disclosed aspartic protease inhibitors.

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    合成参考文献


    摘要:Kantchev, E. A. B.; Organ, M. G., Science of Synthesis, (2009) 48, 38.
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