[(Z)-1-[(E)-2-methoxy-1-methyl-vinyl]prop-1-enoxy]-trimethyl-silane | 82093-19-4

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: [(Z)-1-[(E)-2-methoxy-1-methyl-vinyl]prop-1-enoxy]-trimethyl-silane
• 英文别名: ((1-methoxy-2-methylpenta-1,3-dien-3-yl)oxy)trimethylsilane；1-methoxy-2-methyl-3-(trimethylsilyloxy)-1,3-pentadiene；1-Methoxy-2,4-dimethyl-3-(trimethylsiloxy)butadiene；(1-methoxy-2-methylpenta-1,3-dien-3-yl)oxy-trimethylsilane
• CAS: 82093-19-4
• 化学式: C₁₀H₂₀O₂Si
• 分子量: 200.353
• InChiKey: SSGAQVOLXCOJGN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.29
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  [(Z)-1-[(E)-2-methoxy-1-methyl-vinyl]prop-1-enoxy]-trimethyl-silane 在 盐酸 、 三乙基硅烷 、 sodium borohydrid 作用下， 以 甲醇 、 氘代氯仿 为溶剂， 生成 5-(3,5-dimethyl-3,6-dihydro-2H-pyran-2-yl)-1-methyl-4-nitro-pyrazole
  参考文献：
  名称：

  CYCLIC ETHER PYRAZOL-4-YL-HETEROCYCLYL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE

  摘要：

  公式I的环醚吡唑-4-基-杂环基-羧酰胺化合物，包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐，其中R2为环醚，X为噻唑基、吡啶基、吡啶基或嘧啶基，可用于抑制Pim激酶，并用于治疗由Pim激酶介导的癌症等疾病。公开了使用公式I化合物进行体外、体内和体内诊断、预防或治疗哺乳动物细胞中的这类疾病或相关病理条件的方法。

  公开号：

  US20140088117A1

文献信息

• Diverted Total Synthesis Leads to the Generation of Promising Cell-Migration Inhibitors for Treatment of Tumor Metastasis: <i>In vivo</i> and Mechanistic Studies on the Migrastatin Core Ether Analog
  作者：Thordur Oskarsson、Pavel Nagorny、Isaac J. Krauss、Lucy Perez、Mihirbaran Mandal、Guangli Yang、Ouathek Ouerfelli、Danhua Xiao、Malcolm A. S. Moore、Joan Massagué、Samuel J. Danishefsky

  DOI：10.1021/ja9101503

  日期：2010.3.10

  A significantly simpler analog of the natural product migrastatin, termed migrastatin ether (ME), has been prepared and evaluated. Both in vivo and in vitro studies indicate that ME exhibits a concentration-dependent inhibitory effect on migration of breast cancer cells.

  已制备并评估了一种明显更简单的天然产物 migrastatin 类似物，称为 migrastatin ether (ME)。体内和体外研究表明，ME 对乳腺癌细胞的迁移具有浓度依赖性抑制作用。
• A New Approach to Di- and Tetrasubstituted 2,3-Dihydropyridin-4(1H)-ones through Aza-Diels-Alder Reaction Promoted by Silicon Tetrachloride
  作者：Antonio Massa、Vincenzo de Sio、Rosaria Villano、M. Acocella、Laura Palombi、Giusi Sellitto、Antonella Peduto、Rosanna Filosa、Paolo De Capraris、Arrigo Scettri

  DOI：10.1055/s-0028-1087677

  日期：2009.2

  Silicon tetrachloride promotes an aza-Diels-Alder reaction with a range of imines and Danishefsky’s diene or an alkylated derivative, giving the desired products in good to excellent yields. aza-Diels-Alder reaction - heterocycles - silicon tetrachloride

  四氯化硅可促进与一系列亚胺和Danishefsky的二烯或烷基化衍生物的aza-Diels-Alder反应，以高至极好的收率获得所需的产物。 氮杂-狄尔斯-阿尔德反应-杂环-四氯化硅
• Lewis Base Catalyzed Aza-Diels-Alder Type Reactions between Danishefsky’s Dienes in the Presence of Lewis Base Catalysts. An Efficient Method for the Synthesis of Substituted 2,3-Dihydropyridin-4-ones
  作者：Takayuki Kitazawa、Yuji Maruyama、Teruaki Mukaiyama

  DOI：10.3987/com-07-s(u)65

  日期：——

  Aza-Diels-Alder type reactions of various imines with 1-methoxy-3-trimethylsilyloxy-1,3-butadiene (Danishefsky's diene) derivatives catalyzed by Lewis bases such as lithium methoxide are described. The reaction proceeds via a stepwise pathway, i.e. first by an imino-aldol reaction followed by the acid mediated annulation to afford the corresponding 2,3-dihydropyridin-4-ones in high yields. An appropriate

  描述了各种亚胺与 1-methoxy-3-trimethylsilyloxy-1,3-butadiene (Danishefsky's diene) 衍生物的 Aza-Diels-Alder 型反应，这些反应由 Lewis 碱如甲醇锂催化。该反应通过逐步途径进行，即首先通过亚氨基-羟醛反应，然后是酸介导的环化，以高产率提供相应的2,3-二氢吡啶-4-酮。An appropriate choice of the substituents on nitrogen plays important roles both in addition of the silyl enolates and in the subsequent annulation to form the desired cycloadducts.
• Highly Enantioselective Hetero-Diels-Alder Reaction of 1,3-Bis(silyloxy)-1,3-dienes with Aldehydes Catalyzed by Chiral Disulfonimide
  作者：Joyram Guin、Constantinos Rabalakos、Benjamin List

  DOI：10.1002/anie.201204262

  日期：2012.8.27

  with F: The title reaction proceeds using 1 mol % of the new perfluoroisopropyl chiral disulfonimide catalyst 1 to deliver several 2,6‐disubstituted and 2,5,6‐trisubstituted dihydropyrones in good yields and with excellent enantiomeric ratios. The utility of this methodology is illustrated with the first enantioselective synthesis of a potent aromatase inhibitor.

  与F混合使用：使用1 mol％的新型全氟异丙基手性二磺酰亚胺催化剂1进行标题反应，以高收率和出色的对映体比率提供数个2,6-二取代和2,5,6-三取代的二氢吡喃酮。该方法的实用性通过有效的芳香化酶抑制剂的首次对映选择性合成得到了说明。
• PYRIDONE COMPOUNDS AND AGRICULTURAL AND HORTICULTURAL FUNGICIDES CONTAINING THE SAME AS ACTIVE INGREDIENTS
  申请人：MITSUI CHEMICALS AGRO, INC.

  公开号：US20200196600A1

  公开（公告）日：2020-06-25

  A pyridone compound represented by Formula (1): wherein R1, R2, X, Y and Z are defined. The pyridone compound can control plant diseases.

  一种由化学式（1）表示的吡啶酮化合物：其中R1、R2、X、Y和Z被定义。该吡啶酮化合物可以控制植物疾病。