2-<<(benzyloxy)methyl>(tert-butyl)methylsilyl>-2-propyl-1,3-dithiane | 228575-49-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-<<(benzyloxy)methyl>(tert-butyl)methylsilyl>-2-propyl-1,3-dithiane
• CAS: 228575-49-3
• 化学式: C₂₀H₃₄OS₂Si
• 分子量: 382.707
• InChiKey: QQEFLSLAERDCHL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.53
• 重原子数：
  24.0
• 可旋转键数：
  7.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  9.23
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  2-<<(benzyloxy)methyl>(tert-butyl)methylsilyl>-2-propyl-1,3-dithiane 在 无水碳酸镉 、 lithium (1 percent sodium) 、 1,2-二溴乙烷 、 mercury dichloride 、 magnesium bromide 作用下， 以 乙醚 、 正己烷 、 水 、 丙酮 、 甲苯 、 苯 为溶剂， 反应 2.5h， 生成 (R*,R*,Z)-4-<<(benzyloxy)methyl>(tert-butyl)methylsilyl>hept-2-en-4-ol
  参考文献：
  名称：

  A Novel Stereoselective Reaction Cascade Leading fromα-Silylated Allylic Alcohols to Aldol-Type Products

  摘要：

  The treatment of alpha-silylated allylic alcohols with epoxidizing reagents afforded in a highly stereocontrolled fashion a-silylated aldols. The transformation is proposed to proceed either by a reaction cascade involving stereospecific epoxidation of the allylic-alcohol moiety followed by an acid-supported pinacol-type rearrangement, or by a sequence consisting of a pi-face-selective electrophilic attack at the allylic silane moiety with hyperconjugative stabilization of the evolving carbocation, followed by rearrangement of the thus obtained pentacoordinated silanium ion (see Scheme 3). Depending on the reaction conditions, the pi-face selectivity of the oxidation step is controlled by the: stereogenic C-atom or the more remote Si-center of chirality.

  DOI：

  10.1002/(sici)1522-2675(19990407)82:4<561::aid-hlca561>3.0.co;2-u
• 作为产物：
  描述：

  2-(n-propyl)-1,3-dithiane 、 [(benzyloxy)methyl](tert-butyl)chloro(methyl)silane 在 正丁基锂 作用下， 以 四氢呋喃 、 正戊烷 为溶剂， 以91%的产率得到2-<<(benzyloxy)methyl>(tert-butyl)methylsilyl>-2-propyl-1,3-dithiane
  参考文献：
  名称：

  A Novel Stereoselective Reaction Cascade Leading fromα-Silylated Allylic Alcohols to Aldol-Type Products

  摘要：

  The treatment of alpha-silylated allylic alcohols with epoxidizing reagents afforded in a highly stereocontrolled fashion a-silylated aldols. The transformation is proposed to proceed either by a reaction cascade involving stereospecific epoxidation of the allylic-alcohol moiety followed by an acid-supported pinacol-type rearrangement, or by a sequence consisting of a pi-face-selective electrophilic attack at the allylic silane moiety with hyperconjugative stabilization of the evolving carbocation, followed by rearrangement of the thus obtained pentacoordinated silanium ion (see Scheme 3). Depending on the reaction conditions, the pi-face selectivity of the oxidation step is controlled by the: stereogenic C-atom or the more remote Si-center of chirality.

  DOI：

  10.1002/(sici)1522-2675(19990407)82:4<561::aid-hlca561>3.0.co;2-u