tert-Butyl-((1S,2R,5R)-5-isopropenyl-2-methyl-cyclohexyloxy)-dimethyl-silane | 218268-88-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: tert-Butyl-((1S,2R,5R)-5-isopropenyl-2-methyl-cyclohexyloxy)-dimethyl-silane
• 英文别名: tert-butyl-dimethyl-[(1S,2R,5R)-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxysilane
• CAS: 218268-88-3
• 化学式: C₁₆H₃₂OSi
• 分子量: 268.515
• InChiKey: HNYGMXGILQEZMC-KFWWJZLASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.39
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  tert-Butyl-((1S,2R,5R)-5-isopropenyl-2-methyl-cyclohexyloxy)-dimethyl-silane 在 4-二甲氨基吡啶 、 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 sodium hydroxide 、 sodium hypochlorite 、 臭氧 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 生成 (3S,4R)-3-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-cyclohexanone
  参考文献：
  名称：

  Bioreduction of (R)-carvone and regioselective Baeyer-Villiger oxidations: Application to the asymmetric synthesis of cryptophycin fragment A

  摘要：

  Cryptophycin fragment A (1) was prepared in high enantiomeric purity in 10 steps from(R)-carvone. A stereoselective bioreduction of (R)-carvone to neodihydrocarveol and a regioselective Baeyer-Villiger oxidation of cyclohexanone 8 with pertrifluoroacetic acid were employed in this synthesis. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(98)01784-5
• 作为产物：
  描述：

  (+)-二氢香芹酮 在 L-Selectride 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 tert-Butyl-((1S,2R,5R)-5-isopropenyl-2-methyl-cyclohexyloxy)-dimethyl-silane
  参考文献：
  名称：

  Bioreduction of (R)-carvone and regioselective Baeyer-Villiger oxidations: Application to the asymmetric synthesis of cryptophycin fragment A

  摘要：

  Cryptophycin fragment A (1) was prepared in high enantiomeric purity in 10 steps from(R)-carvone. A stereoselective bioreduction of (R)-carvone to neodihydrocarveol and a regioselective Baeyer-Villiger oxidation of cyclohexanone 8 with pertrifluoroacetic acid were employed in this synthesis. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(98)01784-5

文献信息

• Bioreduction of (R)-carvone and regioselective Baeyer-Villiger oxidations: Application to the asymmetric synthesis of cryptophycin fragment A
  作者：David L. Varie、John Brennan、Barbara Briggs、Jason S. Cronin、David A. Hay、John A. Rieck、Milton J. Zmijewski

  DOI：10.1016/s0040-4039(98)01784-5

  日期：1998.11

  Cryptophycin fragment A (1) was prepared in high enantiomeric purity in 10 steps from(R)-carvone. A stereoselective bioreduction of (R)-carvone to neodihydrocarveol and a regioselective Baeyer-Villiger oxidation of cyclohexanone 8 with pertrifluoroacetic acid were employed in this synthesis. (C) 1998 Elsevier Science Ltd. All rights reserved.