CAS: 171364-81-1; 1-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Phenyl)Ethanone

该化合物是一种多用途的博龙酸衍生物,在有机合成中可以增强回活动性和选择性. 它的独特结构有利于铃木高效的组合反应,为构建碳-碳债券提供了强有力的工具. 平聚醇酯组增加了处理的稳定性和方便性,使它成为医学化学和材料科学领域的研究人员的有吸引力的选择.

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相似化合物

149104-90-5 128376-64-7 1256359-22-4

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合成工艺路线路线简述

    📜4-乙酰基苯甲酰氯置于4-二甲氨基吡啶,Wilkinson'S Catalyst,三乙胺体系中,用 二氯甲烷,甲苯 用作溶剂,化学反应 27.0H,反应生成4-乙酰苯基硼酸,醇酯
    参考文献:Rh催化的酰胺酰胺的无碱脱羰基硼化反应
    标题:Rh催化的酰胺酰胺的无碱脱羰基硼化反应
    摘要:我们报告了铑催化的酰胺的无碱脱羰基硼化.由芳基扭曲酰胺合成通用的芳基硼酸酯是通过脱羰铑(i)催化和高度选择性的n-c(o)插入来实现的.该方法在非常实用的无添加剂rh(i)催化剂体系中非常引人注目.该方法显示出宽泛的官能团耐受性和出色的底物范围,包括通过不同的n-C / C-Br裂解和后期药物硼化进行的位点选择性脱羰基硼化/ Heck交叉偶联.
    Doi:10.1021/acs.Joc.0C02157

    海关参考信息

    专利信息


    专利号:US-2014228303-A1
    优先权日:2011-06-13
    标题 :Novel sglt inhibitors
    发明人:JAIN RAJESH; TREHAN SANJAY; DAS JAGATTARAN; NANDA GURMEET KAUR; THUNGATHURTHI SASTRY V R S; SINGH NISHAN; SHARMA SUDHIR KUMAR
    权利人:JAIN RAJESH; TREHAN SANJAY; DAS JAGATTARAN; NANDA GURMEET KAUR; THUNGATHURTHI SASTRY V R S; SINGH NISHAN; SHARMA SUDHIR KUMAR; PANACEA BIOTEC LTD
    摘要:The present invention relates to novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, isomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The invention also relates to the processes for the synthesis of novel compounds of Formula I, their pharmaceutically acceptable derivatives, tautomeric forms, isomers, polymorphs, prodrugs, metabolites, salts or solvates thereof. The present invention also provides pharmaceutical compositions comprising novel compounds of Formula I and methods of treating or preventing one or more conditions or diseases that may be regulated or normalized via inhibition of Sodium Glucose Cotransporter-2 (SGLT-2).

    专利号:CN-113956274-A
    优先权日:2021-10-29
    标 题:Design and synthesis of a fluorescent probe dual-responsive to changes in viscosity and peroxynitrite in epilepsy disease

    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


    摘要:Suginome, M.; Ohmura, T., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 160.
    摘要:Murata, M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 449.
    摘要:Murata, M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 440.
    摘要:Geetharani, K.; Bose, S. K., Science of Synthesis: Advances in Organoboron Chemistry towards Organic Synthesis, (2019) 1, 347.
    摘要:Yoshida, H., Science of Synthesis: Advances in Organoboron Chemistry towards Organic Synthesis, (2019) 1, 61.
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