(3aR,5R,6S,6aR)-2,2-dimethyl-5-[5-[(2S)-oxiran-2-yl]pentyl]-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole | 912352-00-2

• 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: (3aR,5R,6S,6aR)-2,2-dimethyl-5-[5-[(2S)-oxiran-2-yl]pentyl]-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole
• CAS: 912352-00-2
• 化学式: C₂₁H₃₀O₅
• 分子量: 362.466
• InChiKey: RSDFPLQZKZUTKR-PXTPFGJHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  26
• 可旋转键数：
  9
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  49.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (3aR,5R,6S,6aR)-2,2-dimethyl-5-[5-[(2S)-oxiran-2-yl]pentyl]-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole 在 4-二甲氨基吡啶 、 lithium aluminium tetrahydride 、 溶剂黄146 、 高碘酸 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 、 乙酸乙酯 、 甲苯 为溶剂， 反应 18.0h， 生成 [(E,2R,8R,9R)-8-formyloxy-12-methoxy-12-oxo-9-phenylmethoxydodec-10-en-2-yl] benzoate
  参考文献：
  名称：

  Attempts directed towards the synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C

  摘要：

  Attempts to synthesise iso-cladospolide-B, cladospolide-B and cladospolide-C resulted in macrolides 1, 2 and 4 along with butenolide 3. Of the three stereogenic centres, the C-4/C-5 vic-diol was obtained from tartaric acid and D-glucose, while the C-11 stereocentre was created by Jacobsen's method. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.07.043
• 作为产物：
  描述：

  tert-butyl-(5-iodo-pentyloxy)-diphenyl-silane 在 platinum(IV) oxide 、 (S,S)-(salen)manganese 正丁基锂 、 草酰氯 、 potassium tert-butylate 、 四丁基氟化铵 、 氢气 、 二甲基亚砜 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 、 二甲基亚砜 、 乙酸乙酯 、 甲苯 为溶剂， 反应 65.0h， 生成 (3aR,5R,6S,6aR)-2,2-dimethyl-5-[5-[(2S)-oxiran-2-yl]pentyl]-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole
  参考文献：
  名称：

  Attempts directed towards the synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C

  摘要：

  Attempts to synthesise iso-cladospolide-B, cladospolide-B and cladospolide-C resulted in macrolides 1, 2 and 4 along with butenolide 3. Of the three stereogenic centres, the C-4/C-5 vic-diol was obtained from tartaric acid and D-glucose, while the C-11 stereocentre was created by Jacobsen's method. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.07.043

文献信息

• Attempts directed towards the synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C
  作者：G.V.M. Sharma、J. Janardhan Reddy、K. Laxmi Reddy

  DOI：10.1016/j.tetlet.2006.07.043

  日期：2006.9

  Attempts to synthesise iso-cladospolide-B, cladospolide-B and cladospolide-C resulted in macrolides 1, 2 and 4 along with butenolide 3. Of the three stereogenic centres, the C-4/C-5 vic-diol was obtained from tartaric acid and D-glucose, while the C-11 stereocentre was created by Jacobsen's method. (c) 2006 Elsevier Ltd. All rights reserved.