CAS: 80866-93-9; 2,2-Dimethyl-4-Oxo-3,4-Dihydro-2H-Pyran-6-Carboxylic Acid

该化合物是一种多用途的环环碳酸,其主脊有皮兰,广泛用于有机合成和制药中间体,其结构特征,包括2,2-二甲基和4-氧功能组,有助于其稳定性和反应性,使之适合用于细化化学制造;该化合物是生物活性分子合成的主要前体,特别是在农用化学和药用化合物的开发方面;其定义明确的化学特性和高纯度确保复杂反应的性能一致;该酸与各种联动和凝聚反应的兼容性进一步提高其在研究和工业应用中的效用.

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108799-25-3 520-45-6 5464-36-8

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CAS号108097-78-5 hydroxy-2 oxo-4...

合成工艺路线路线简述

  • 5464-36-8 = 80866-93-9
    反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Tetrahydrofuran,Water; 24 H,Rt
    标题:Metal-Free Visible Light-Mediated Photocatalysis: Controlling Intramolecular [2 + 2] Photocycloaddition Of Enones Through Axial Chirality
    作者:Clay,Anthony; Vallavoju,Nandini; Krishnan,Retheesh; Ugrinov,Angel; Sivaguru,Jayaraman
    参考文献:Journal Of Organic Chemistry 日期:2016 卷标:81(16) 页码:7191-7200
📜4-甲基-3戊烯-2-酮置于盐酸体系中,用 四氢呋喃,乙醇,水 作为反应溶剂,化学反应 20.58H,反应生成 3,4-二氢-2,2-二甲基-4-氧代-2H-吡喃-6-羧酸
参考文献:无金属可见光介导的光催化:通过轴向手性控制分子内[2 + 2]烯酮的光环加成反应
标题:无金属可见光介导的光催化:通过轴向手性控制分子内[2 + 2]烯酮的光环加成反应
摘要:对分子特征为[2 + 2]的光环加成反应,评估了具有n-C芳基键旋转特性的对映异构烯酮-酰亚胺和烯酮-酰胺.观测到与交叉加成产物相比,直加成产物具有对反应性的非常好控制.发现阻转选择性取决于芳基环上的取代基.在不同的机理途径的基础上合理化了取代相关的阻转选择性.
DOI:10.1021/acs.Joc.6B01066

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专利信息


专利号:US-7109377-B2
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
权利人:HARVARD COLLEGE
摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

专利号:US-6531470-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

专利号:US-2003082830-A1
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:WO-0006525-A9
优先权日:1998-07-25
标题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:WO-0006525-A2
优先权日:1998-07-25
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

专利号:US-6562844-B2
优先权日:1998-01-23
标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

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合成参考文献


摘要:Farmaco, Edizione Scientifica., 42(145), 1987 []
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