CAS: 106921-60-2; 2,2-Dimethyl-3-Oxopentanal

该化合物是一种多用途甲醛酮混合化合物,其特点是具有反应性碳基功能.其结构中存在甲醛和甲酮组,能够将其用作有机合成的关键中间体,特别是在形成异环循环和复杂的分子框架方面.两个甲基组在2级设置的不育障碍增强了某些反应的选择性,而牛开丹骨骼则为进一步衍生提供了灵活性.该化合物在制药和农用化学研究中很有价值,可将其再活性用于开发新型活性成分.在受控制的条件下,其稳定性确保了合成应用的一贯性能.

结构式图片

相似化合物

1118-71-4 3142-58-3 37719-03-2

合成工艺路线路线简述

    📜(+/-)-4,4-Dimethylhex-5-En-3-Ol置于戴斯-马丁氧化剂,臭氧体系中,用 甲醇,二氯甲烷 用作溶剂,化学反应 6.0H,反应生成2,2-二甲基-3-氧代戊醛
    参考文献:通过有机硼烷合成埃博霉素a的研究.
    标题:通过有机硼烷合成埃博霉素a的研究.
    摘要:已经描述了通过有机硼烷合成埃坡霉素a的研究.已开发出一种从异戊烯醇大规模制备b-γ,γ-二甲基烯丙基亚砜基樟脑基硼烷的改进方法.与各种醛反应后,该试剂以高对映选择性提供相应的α,α-二甲基均烯丙基醇.已经证明了该试剂在合成埃博霉素的c1-C6亚基中的应用.或者,分子间和分子内不对称还原方案也已用于合成埃坡霉素a的c1-C6亚基.使用α-Pine烯衍生的试剂合成埃坡霉素a的c7-C21片段,涉及不对称烷氧基烯丙基和巴豆基硼化也已经描述过了.
    Doi:10.1039/b508001K

    专利信息


    专利号:US-6350878-B1
    优先权日:1998-05-18
    标 题 :Intermediates for the synthesis of epothilones and methods for their preparation
    发明人:ALTMANN KARL-HEINZ; BAUER ARMIN; SCHINZER DIETER
    权利人:NOVARTIS AG
    摘要:The invention relates to a method of synthesis for a compound of formula (I),wherein R is a heterocyclyl moiety and X1, X2, X3 and X4 are, independently of each other, protecting groups, which is appropriate for the synthesis of epothilone B and desoxyepothione B.

    专利号:US-2003176368-A1
    优先权日:2001-09-06
    标题:Synthesis of epothilones, intermediates thereto and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; BISWAS KAUSTAV; CHAPPELL MARK; LIN HONG; NJARDARSON JON T; LEE CHUL BOM; RIVKIN ALEXY; CHOU TING-CHAO
    摘要:The present invention provides compounds of formula (I): n n n as described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).

    专利号:US-2002058286-A1
    优先权日:1999-02-24
    标 题 :Synthesis of epothilones, intermediates thereto and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; STACHEL SHAWN J; LEE CHUL BOM; CHAPPELL MARK D; CHOU TING-CHAO; WU ZHICAI
    摘要:The present invention provides convergent processes for preparing epothilones, desoxyepothilones, and analogues thereof. The present invention further provides novel compositions and methods for the treatment of cancer and additionally provides methods for the treatment of cancer which has developed a multi-drug phenotype.

    专利号:US-6867305-B2
    优先权日:1996-12-03
    标题:Synthesis of epothilones, intermediates thereto and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; STACHEL SHAWN J; LEE CHUL BOM; CHAPPELL MARK D; WU ZHICAL
    权利人:SLOAN KETTERING INST CANCER; UNIV COLUMBIA
    摘要:The present invention provides convergent processes for preparing epothilones, desoxyepothilones, and analogues thereof. The present invention further provides novel compositions and methods for the treatment of cancer and additionally provides methods for the treatment of cancer which has developed a multi-drug phenotype.

    专利号:US-6867333-B2
    优先权日:2000-10-16
    标题:Epothilone synthesis building blocks iii and iv: asymmetrically substituted acyloins and acyloin derivatives, methods for their production and methods for the production of epothilones b, d and epothilone derivatives
    发明人:WESSJOHANN LUDGER A; SCHEID GUNTHER; BORNSCHEUER UWE; HENKE ERIK; KUIT WOUTER; ORRU ROMANO
    权利人:MORPHOCHEM AG
    摘要:The present invention is directed to novel acyloins, their derivatives, methods for their production and their use for the production of novel epothilones and their derivatives. In addition, the invention is directed to the building blocks for epothilone synthesis, methods for their production and the use of synthetic building blocks for the production of epothilones and their derivatives.

    专利号:WO-9959985-A1
    优先权日:1998-05-18
    标题:Intermediates for the synthesis of epothilones and methods for their preparation

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1055/s-2007-968281
    摘要:Jamison T, Moslin R. Synthesis of (+)-Acutiphycin. Synfacts. 2007 Apr;2007(4):0347. doi: 10.1055/s-2007-968281.
    参考文献:10.1055/s-2005-872698
    摘要:Dixon DJ, Scott MS, Luckhurst CA. Ligand-Mediated Enantioselective Synthesis of Acyclic Pyrrole Carbinols. Synlett. 2005;(16):2420–4. doi: 10.1055/s-2005-872698.
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