tert-Butyl-[(4Z,8E)-(1S,7S,11S)-7,11-dimethyl-7-(4-methyl-pent-3-enyl)-12-oxa-bicyclo[9.1.0]dodeca-4,8-dien-4-ylmethoxy]-dimethyl-silane | 609767-84-2

• 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: tert-Butyl-[(4Z,8E)-(1S,7S,11S)-7,11-dimethyl-7-(4-methyl-pent-3-enyl)-12-oxa-bicyclo[9.1.0]dodeca-4,8-dien-4-ylmethoxy]-dimethyl-silane
• 英文别名: tert-butyl-[[(1S,4Z,7S,8E,11S)-7,11-dimethyl-7-(4-methylpent-3-enyl)-12-oxabicyclo[9.1.0]dodeca-4,8-dien-4-yl]methoxy]-dimethylsilane
• CAS: 609767-84-2
• 化学式: C₂₆H₄₆O₂Si
• 分子量: 418.736
• InChiKey: FSXFICITZVPPQO-LBPRJKNDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.98
• 重原子数：
  29
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.77
• 拓扑面积：
  21.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  tert-Butyl-[(4Z,8E)-(1S,7S,11S)-7,11-dimethyl-7-(4-methyl-pent-3-enyl)-12-oxa-bicyclo[9.1.0]dodeca-4,8-dien-4-ylmethoxy]-dimethyl-silane 在 四丁基氟化铵 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 生成 (4Z,8E)-(1S,7S,11S)-7,11-Dimethyl-7-(4-methyl-pent-3-enyl)-12-oxa-bicyclo[9.1.0]dodeca-4,8-diene-4-carbaldehyde
  参考文献：
  名称：

  Determination of the absolute configuration of vibsanin F by asymmetric synthesis via π-allylpalladium complex

  摘要：

  The absolute configuration of vibsanin F (1), one of the simplest 11-membered ring vibsane-type diterpene, was established to be 6R, 7S and 11S by asymmetric synthesis. A diastereomer (1a) with a 6S, 7S and 11S configuration was synthesized starting from myrcene by procedures featuring a Sharpless asymmetric epoxidation and a high diastereoselective eleven-membered ring formation between a pi-allylpalladium complex and a beta-ketoester nucleophile. Subsequent reduction of epoxide in la with LiAlH4 gave a diol, which was identical with that derived from vibsanin F. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(03)01537-5
• 作为产物：
  描述：

  8-羟基-7-甲基-3-亚甲基-1,6-(E)-辛二烯 在 titanium(IV) isopropylate 、 四(三苯基膦)钯 叔丁基过氧化氢 、 4-二甲氨基吡啶 、 N,N-二甲基丙烯基脲 、 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 15-冠醚-5 、 L-(+)-酒石酸二乙酯 、 三氟甲磺酸酐 、 4 A molecular sieve 、 sodium hydride 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 二氯甲烷 、 二甲基亚砜 、 甲苯 为溶剂， 生成 tert-Butyl-[(4Z,8E)-(1S,7S,11S)-7,11-dimethyl-7-(4-methyl-pent-3-enyl)-12-oxa-bicyclo[9.1.0]dodeca-4,8-dien-4-ylmethoxy]-dimethyl-silane
  参考文献：
  名称：

  Determination of the absolute configuration of vibsanin F by asymmetric synthesis via π-allylpalladium complex

  摘要：

  The absolute configuration of vibsanin F (1), one of the simplest 11-membered ring vibsane-type diterpene, was established to be 6R, 7S and 11S by asymmetric synthesis. A diastereomer (1a) with a 6S, 7S and 11S configuration was synthesized starting from myrcene by procedures featuring a Sharpless asymmetric epoxidation and a high diastereoselective eleven-membered ring formation between a pi-allylpalladium complex and a beta-ketoester nucleophile. Subsequent reduction of epoxide in la with LiAlH4 gave a diol, which was identical with that derived from vibsanin F. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(03)01537-5

文献信息

• Determination of the absolute configuration of vibsanin F by asymmetric synthesis via π-allylpalladium complex
  作者：Hiroaki Yuasa、Gouki Makado、Yoshiyasu Fukuyama

  DOI：10.1016/s0040-4039(03)01537-5

  日期：2003.8

  The absolute configuration of vibsanin F (1), one of the simplest 11-membered ring vibsane-type diterpene, was established to be 6R, 7S and 11S by asymmetric synthesis. A diastereomer (1a) with a 6S, 7S and 11S configuration was synthesized starting from myrcene by procedures featuring a Sharpless asymmetric epoxidation and a high diastereoselective eleven-membered ring formation between a pi-allylpalladium complex and a beta-ketoester nucleophile. Subsequent reduction of epoxide in la with LiAlH4 gave a diol, which was identical with that derived from vibsanin F. (C) 2003 Elsevier Ltd. All rights reserved.