(6R,Z)-6-[3-{2-benzyloxy-4-(tert-butyldiphenylsilanyloxy)phenyl}-1-{(2-methoxyethoxy)methoxy}-2-propen-2-yl]-3-methyl-1,4,4a,5,6,7-hexahydronaphthalen-4a-ol | 1115267-06-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (6R,Z)-6-[3-{2-benzyloxy-4-(tert-butyldiphenylsilanyloxy)phenyl}-1-{(2-methoxyethoxy)methoxy}-2-propen-2-yl]-3-methyl-1,4,4a,5,6,7-hexahydronaphthalen-4a-ol
• CAS: 1115267-06-5
• 化学式: C₄₇H₅₆O₆Si
• 分子量: 745.044
• InChiKey: SLPYJEJSFKQEFA-XERZOQHESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.03
• 重原子数：
  54.0
• 可旋转键数：
  16.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  66.38
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  (1R,3RS,5R,Z)-5-{3-[2-benzyloxy-4-(tert-butyldiphenylsilanyloxy)-phenyl]-1-[(2-methoxyethoxy)methoxy]-2-propen-2-yl}-3-(2-methyl-2-propen-1-yl)-2-methylene-3-trimethylsilanyloxy-1-cyclohexanol 在 吡啶 、 甲基磺酰氯 作用下， 以 二氯甲烷 为溶剂， 以16%的产率得到(6R,Z)-6-[3-{2-benzyloxy-4-(tert-butyldiphenylsilanyloxy)phenyl}-1-{(2-methoxyethoxy)methoxy}-2-propen-2-yl]-3-methyl-1,4,4a,5,6,7-hexahydronaphthalen-4a-ol
  参考文献：
  名称：

  Synthetic studies toward miroestrols: trials for elongation of the methyl group of 5-substituted 2-methyl-2-cyclohexanone to 3-methyl-2-butenyl function

  摘要：

  Toward total synthesis of miroestrols (miroestrol and deoxymiroestrol), 3-methyl-2-butenyl function (endo-C5 unit) on D ring as a carbon chain for C and E rings was prepared by elongation of the methyl group in alpha-methyl-alpha.,beta-unsaturated ketone unit, and 3,5-dinitrobenzoyl group was introduced as a potential leaving group for the construction of B ring. The former was accomplished through a sequence of epoxide ring-opening, microwave-irradiated siloxy-Cope rearrangement, and isomerization of 3-methyl-3-butenyl function (exo-C5 unit) to endo-C5 unit. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2008.11.055