(Z)-6-(tert-butyldiphenylsilyloxy)-3-methylhex-2-en-1-ol | 917611-85-9

• 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)-6-(tert-butyldiphenylsilyloxy)-3-methylhex-2-en-1-ol
• 英文别名: (Z)-6-[tert-butyl(diphenyl)silyl]oxy-3-methylhex-2-en-1-ol
• CAS: 917611-85-9
• 化学式: C₂₃H₃₂O₂Si
• 分子量: 368.591
• InChiKey: KOWZZZBJFWAADM-JZJYNLBNSA-N

物化性质

• 沸点：
  448.5±45.0 °C(Predicted)
• 密度：
  1.01±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.28
• 重原子数：
  26
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (Z)-6-(tert-butyldiphenylsilyloxy)-3-methylhex-2-en-1-ol 在 18-冠醚-6 、 四丁基氟化铵 、 三乙胺 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 反应 48.0h， 生成 (Z)-5-methyl-8-m-tolyloct-5-enenitrile
  参考文献：
  名称：

  Catalytic Diastereoselective Polycyclization of Homo(polyprenyl)arene Analogues Bearing Terminal Siloxyvinyl Groups

  摘要：

  Highly diastereoselective polycyclization of homo(polyprenyl) arene analogues bearing terminal siloxyvinyl groups was catalyzed by tin(IV) chloride (10 mol %). The cyclizations of tert-butyldiphenylsilyl and triisopropylsilyl polyenol ethers gave 4 alpha(equatorial)- and 4 beta(axial)-siloxypolycycles as major isomers, respectively. The strong nucleophilicity of pro-C(9), a (6E) geometry, and a bulky silyl group effectively favored the 4 alpha-preference, whereas the weak nucleophilicity of pro-C(9), a (6Z)-geometry, and less steric hindrance of a silyl group favored the 4 beta-preference.

  DOI：

  10.1021/ol062378t
• 作为产物：
  描述：

  橙花醇 在 吡啶 、 sodium tetrahydroborate 、 二异丁基氢化铝 、 臭氧 、 溶剂黄146 、 锌 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 甲苯 为溶剂， 反应 6.0h， 生成 (Z)-6-(tert-butyldiphenylsilyloxy)-3-methylhex-2-en-1-ol
  参考文献：
  名称：

  Transannular Diels-Alder reaction studies with an activated dienophile. An enantioselective synthesis of an A.B.C.[6.6.6] trans-syn-cis tricycle

  摘要：

  The synthesis and transannular Diels-Alder reaction of a chiral 14 membered trans-cis-cis (TCC) macrocyclic triene with an activated dienophile leading to an A.B.C.[6.6.6.] tricyclic compound are described. The outcome of the TADA reaction under thermal and catalyzed conditions is discussed. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00997-6

文献信息

• Catalytic Diastereoselective Polycyclization of Homo(polyprenyl)arene Analogues Bearing Terminal Siloxyvinyl Groups
  作者：Muhammet Uyanik、Kazuaki Ishihara、Hisashi Yamamoto

  DOI：10.1021/ol062378t

  日期：2006.11.1

  Highly diastereoselective polycyclization of homo(polyprenyl) arene analogues bearing terminal siloxyvinyl groups was catalyzed by tin(IV) chloride (10 mol %). The cyclizations of tert-butyldiphenylsilyl and triisopropylsilyl polyenol ethers gave 4 alpha(equatorial)- and 4 beta(axial)-siloxypolycycles as major isomers, respectively. The strong nucleophilicity of pro-C(9), a (6E) geometry, and a bulky silyl group effectively favored the 4 alpha-preference, whereas the weak nucleophilicity of pro-C(9), a (6Z)-geometry, and less steric hindrance of a silyl group favored the 4 beta-preference.
• Transannular Diels-Alder reaction studies with an activated dienophile. An enantioselective synthesis of an A.B.C.[6.6.6] trans-syn-cis tricycle
  作者：Louis Barriault、Stéphane G. Ouellet、Pierre Deslongchamps

  DOI：10.1016/s0040-4020(97)00997-6

  日期：1997.11

  The synthesis and transannular Diels-Alder reaction of a chiral 14 membered trans-cis-cis (TCC) macrocyclic triene with an activated dienophile leading to an A.B.C.[6.6.6.] tricyclic compound are described. The outcome of the TADA reaction under thermal and catalyzed conditions is discussed. (C) 1997 Elsevier Science Ltd.