(1S,2R,4S,5S,7E)-2-(methoxymethoxy)-5-<(2S,4R,5S)-2-(p-methoxyphenyl)-5-<<2-(trimethylsilyl)ethoxy>methoxy>-4-vinyl-m-dioxan-5-yl>-4,11,11-trimethylbicyclo<6.2.1>undec-7-en-3-one | 217820-17-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (1S,2R,4S,5S,7E)-2-(methoxymethoxy)-5-<(2S,4R,5S)-2-(p-methoxyphenyl)-5-<<2-(trimethylsilyl)ethoxy>methoxy>-4-vinyl-m-dioxan-5-yl>-4,11,11-trimethylbicyclo<6.2.1>undec-7-en-3-one
• 英文别名: (1S,2R,4S,5S,7E)-5-[(2S,4R,5S)-4-ethenyl-2-(4-methoxyphenyl)-5-(2-trimethylsilylethoxymethoxy)-1,3-dioxan-5-yl]-2-(methoxymethoxy)-4,11,11-trimethylbicyclo[6.2.1]undec-7-en-3-one
• CAS: 217820-17-2
• 化学式: C₃₅H₅₄O₈Si
• 分子量: 630.894
• InChiKey: GPCJAQWPPNDMOT-XFDVNUDISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.94
• 重原子数：
  44
• 可旋转键数：
  13
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.69
• 拓扑面积：
  81.7
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (1S,2R,4S,5S,7E)-2-(methoxymethoxy)-5-<(2S,4R,5S)-2-(p-methoxyphenyl)-5-<<2-(trimethylsilyl)ethoxy>methoxy>-4-vinyl-m-dioxan-5-yl>-4,11,11-trimethylbicyclo<6.2.1>undec-7-en-3-one 在 吡啶 、 四氧化锇 作用下， 反应 2.0h， 以41%的产率得到(1S,2R,4S,5S,7S,8S)-7,8-dihydroxy-2-(methoxymethoxy)-5-<(2S,4R,5S)-2-(p-methoxyphenyl)-5-<<2-(trimethylsilyl)ethoxy>methoxy>-4-vinyl-m-dioxan-5-yl>-4,11,11-trimethylbicyclo<6.2.1>undecan-3-one
  参考文献：
  名称：

  Stereochemical Models for the Enantiocontrolled Construction of Fully Functionalized C Rings via Intramolecular Aldolization in Advanced Precursors to Paclitaxel

  摘要：

  Six transition-state models for intramolecular aldol C-ring annulation in suitably substituted bicyclo-[6.2.1]undecanones have been defined. The first consideration is the inherent conformational flexibility of the nine-membered ketonic ring which does not limit effective deprotonation to a single C-8 epimer. When the oxygen substituents at C-4 and C-5 are not covalently linked, the configuration at C-5 defines the stereochemical course of the ring closure, with only the beta series being amenable to the proper elaboration of paclitaxel. When C-4 and C-5 are incorporated into a 1,3-dioxane ring instead, the principal stereocontrol element is translocated into the aryl-substituted carbon of the cyclic acetal. To the extent that the Ar group remains equatorially disposed, then proper aldolization will materialize in only one of the four possible diastereomers. Experimental tests that are provided for three of the models are shown to conform to expectations. This analysis of the origin of stereoselectivity has, for the first time, defined the scope and limitations associated with C-ring closure by means of the aldol protocol.

  DOI：

  10.1021/jo981749j
• 作为产物：
  描述：

  (2S,4R,5S)-2-(4-Methoxy-phenyl)-5-(2-trimethylsilanyl-ethoxymethoxy)-4-vinyl-[1,3]dioxane-5-carbaldehyde 在 正丁基锂 、 18-冠醚-6 、 sodium hexamethyldisilazane 、 双(三甲基硅烷基)氨基钾 作用下， 反应 2.58h， 生成 (1S,2R,4S,5S,7E)-2-(methoxymethoxy)-5-<(2S,4R,5S)-2-(p-methoxyphenyl)-5-<<2-(trimethylsilyl)ethoxy>methoxy>-4-vinyl-m-dioxan-5-yl>-4,11,11-trimethylbicyclo<6.2.1>undec-7-en-3-one
  参考文献：
  名称：

  Stereochemical Models for the Enantiocontrolled Construction of Fully Functionalized C Rings via Intramolecular Aldolization in Advanced Precursors to Paclitaxel

  摘要：

  Six transition-state models for intramolecular aldol C-ring annulation in suitably substituted bicyclo-[6.2.1]undecanones have been defined. The first consideration is the inherent conformational flexibility of the nine-membered ketonic ring which does not limit effective deprotonation to a single C-8 epimer. When the oxygen substituents at C-4 and C-5 are not covalently linked, the configuration at C-5 defines the stereochemical course of the ring closure, with only the beta series being amenable to the proper elaboration of paclitaxel. When C-4 and C-5 are incorporated into a 1,3-dioxane ring instead, the principal stereocontrol element is translocated into the aryl-substituted carbon of the cyclic acetal. To the extent that the Ar group remains equatorially disposed, then proper aldolization will materialize in only one of the four possible diastereomers. Experimental tests that are provided for three of the models are shown to conform to expectations. This analysis of the origin of stereoselectivity has, for the first time, defined the scope and limitations associated with C-ring closure by means of the aldol protocol.

  DOI：

  10.1021/jo981749j

文献信息

• Stereochemical Models for the Enantiocontrolled Construction of Fully Functionalized C Rings via Intramolecular Aldolization in Advanced Precursors to Paclitaxel
  作者：Leo A. Paquette、Qingbei Zeng、Hon-Chung Tsui、Jeffrey N. Johnston

  DOI：10.1021/jo981749j

  日期：1998.11.1

  Six transition-state models for intramolecular aldol C-ring annulation in suitably substituted bicyclo-[6.2.1]undecanones have been defined. The first consideration is the inherent conformational flexibility of the nine-membered ketonic ring which does not limit effective deprotonation to a single C-8 epimer. When the oxygen substituents at C-4 and C-5 are not covalently linked, the configuration at C-5 defines the stereochemical course of the ring closure, with only the beta series being amenable to the proper elaboration of paclitaxel. When C-4 and C-5 are incorporated into a 1,3-dioxane ring instead, the principal stereocontrol element is translocated into the aryl-substituted carbon of the cyclic acetal. To the extent that the Ar group remains equatorially disposed, then proper aldolization will materialize in only one of the four possible diastereomers. Experimental tests that are provided for three of the models are shown to conform to expectations. This analysis of the origin of stereoselectivity has, for the first time, defined the scope and limitations associated with C-ring closure by means of the aldol protocol.