(2R,4R)-4-[tert-butyl(dimethyl)silyl]oxy-1-(1,3-dithian-2-yl)heptadecan-2-ol | 1226954-62-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二噻烷
• 英文名称: (2R,4R)-4-[tert-butyl(dimethyl)silyl]oxy-1-(1,3-dithian-2-yl)heptadecan-2-ol
• CAS: 1226954-62-6
• 化学式: C₂₇H₅₆O₂S₂Si
• 分子量: 504.958
• InChiKey: HZZHSNHEVKBRAH-JWQCQUIFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.42
• 重原子数：
  32
• 可旋转键数：
  19
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  80.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (2R,4R)-4-[tert-butyl(dimethyl)silyl]oxy-1-(1,3-dithian-2-yl)heptadecan-2-ol 、 叔丁基二甲基氯硅烷 在 咪唑 作用下， 以 二氯甲烷 为溶剂， 反应 5.0h， 以89%的产率得到tert-butyl-[(2R,4R)-2-[tert-butyl(dimethyl)silyl]oxy-1-(1,3-dithian-2-yl)heptadecan-4-yl]oxy-dimethylsilane
  参考文献：
  名称：

  Stereoselective synthesis of bioactive natural spiroacetals aculeatins A and B

  摘要：

  The stereoselective synthesis of two naturally occurring bioactive spiroacetals, aculeatins A and B has been accomplished using 1-tetradecanal as the starting material. The sequence introduces diastereoselective iodine-induced electrophilic cyclization and ring opening of epoxide with 1,3-dithiane as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.01.162
• 作为产物：
  描述：

  1,3-二噻烷 、 (2R)-2-[(tert-butyldimethylsilyl)oxy]-1-[(2R)-oxiran-2-yl]pentadecane 在 正丁基锂 作用下， 以 四氢呋喃 、 六甲基磷酰三胺 为溶剂， 反应 1.0h， 以86%的产率得到(2R,4R)-4-[tert-butyl(dimethyl)silyl]oxy-1-(1,3-dithian-2-yl)heptadecan-2-ol
  参考文献：
  名称：

  Stereoselective synthesis of bioactive natural spiroacetals aculeatins A and B

  摘要：

  The stereoselective synthesis of two naturally occurring bioactive spiroacetals, aculeatins A and B has been accomplished using 1-tetradecanal as the starting material. The sequence introduces diastereoselective iodine-induced electrophilic cyclization and ring opening of epoxide with 1,3-dithiane as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.01.162

文献信息

• Stereoselective synthesis of bioactive natural spiroacetals aculeatins A and B
  作者：Biswanath Das、Martha Krishnaiah、Chithaluri Sudhakar

  DOI：10.1016/j.bmcl.2010.01.162

  日期：2010.4

  The stereoselective synthesis of two naturally occurring bioactive spiroacetals, aculeatins A and B has been accomplished using 1-tetradecanal as the starting material. The sequence introduces diastereoselective iodine-induced electrophilic cyclization and ring opening of epoxide with 1,3-dithiane as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.