(S,E)-ethyl-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2-methylhex-2-enoate | 1601460-63-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (S,E)-ethyl-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2-methylhex-2-enoate
• CAS: 1601460-63-2
• 化学式: C₁₅H₂₆O₅
• 分子量: 286.368
• InChiKey: XNOXSZJPMKWXRR-UAIPSJAGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.44
• 重原子数：
  20.0
• 可旋转键数：
  7.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  53.99
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  (S,E)-ethyl-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2-methylhex-2-enoate 在 盐酸 、 水 作用下， 以 乙腈 为溶剂， 反应 1.0h， 以96%的产率得到(6S,7R,E)-ethyl 7,8-dihydroxy-6-methoxy-2-methyloct-2-enoate
  参考文献：
  名称：

  Total synthesis of reblastatin: convenient preparation of coupling partners and scaled assembly

  摘要：

  Potentially scalable total synthesis of reblastatin was achieved based on Panek's previous study. Novel and convenient synthetic routes were developed for the known C8-C20 and C1-C7 coupling partners. The challenging C8-C20 fragment was prepared from TBS protected (S)-5-(hydroxymethyl)dihydrofuran-2(3H)-one (6) in nine steps (20% overall yield), and the C1-C7 fragment was synthesized from commercially available 3,4,6-tri-O-acetyl-D-glucal (9) in eight steps (35% overall yield). On a larger scale, Panek's eight-step assembly of the target molecule from the two partners was also slightly modified, giving 45 mg reblastatin (19% overall yield) in the first batch synthesis. Notable feature of our study is the settlement of the C14 chirality through a diastereoselective alpha-alkylation of 6 followed by a three-step full reduction of the lactone carboxyl, making vastly available 6 a universally applicable C11-C14 synthon for benzenoid/benzoquinone ansamycins. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.03.020
• 作为产物：
  描述：

  (6S,7R,E)-ethyl 6,7,8-trihydroxy-2-methyloct-2-enoate 在 4-甲基苯磺酸吡啶 、 1,8-双二甲氨基萘 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 2.5h， 生成 (S,E)-ethyl-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-6-methoxy-2-methylhex-2-enoate
  参考文献：
  名称：

  Total synthesis of reblastatin: convenient preparation of coupling partners and scaled assembly

  摘要：

  Potentially scalable total synthesis of reblastatin was achieved based on Panek's previous study. Novel and convenient synthetic routes were developed for the known C8-C20 and C1-C7 coupling partners. The challenging C8-C20 fragment was prepared from TBS protected (S)-5-(hydroxymethyl)dihydrofuran-2(3H)-one (6) in nine steps (20% overall yield), and the C1-C7 fragment was synthesized from commercially available 3,4,6-tri-O-acetyl-D-glucal (9) in eight steps (35% overall yield). On a larger scale, Panek's eight-step assembly of the target molecule from the two partners was also slightly modified, giving 45 mg reblastatin (19% overall yield) in the first batch synthesis. Notable feature of our study is the settlement of the C14 chirality through a diastereoselective alpha-alkylation of 6 followed by a three-step full reduction of the lactone carboxyl, making vastly available 6 a universally applicable C11-C14 synthon for benzenoid/benzoquinone ansamycins. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.03.020