(2s,3r)-Heptane-1,2,3-Triol | 259656-64-9

• 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: (2s,3r)-Heptane-1,2,3-Triol
• CAS: 259656-64-9
• 化学式: C₇H₁₆O₃
• 分子量: 148.202
• InChiKey: HXYCHJFUBNTKQR-RQJHMYQMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.1
• 重原子数：
  10
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  60.7
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-甲氧基苯乙醛二甲缩醛 、 (2s,3r)-Heptane-1,2,3-Triol 在 camphor-10-sulfonic acid 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以95%的产率得到
  参考文献：
  名称：

  Enantioselective Synthesis of the [6,6] Spiroketal Core of Reveromycin A

  摘要：

  Reveromycin A (1) belongs to a family of microbial polyketides with unusual structural features and biological activities. The structure of 1 is composed of a [6,6] spiroketal core decorated with highly unsaturated side chains, As a prelude to the synthesis of 1, we present herein a short, efficient, and enantioselective synthesis of the C9-C21 fragment 5 (spiroketal core) of reveromycin A.

  DOI：

  10.1021/ol991290v
• 作为产物：
  描述：

  (R)-1-((S)-2,2-Diethyl-[1,3]dioxolan-4-yl)-pentan-1-ol 在 Dowex 50WX-4-400 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 15.0h， 以81%的产率得到(2s,3r)-Heptane-1,2,3-Triol
  参考文献：
  名称：

  Enantioselective Synthesis of the [6,6] Spiroketal Core of Reveromycin A

  摘要：

  Reveromycin A (1) belongs to a family of microbial polyketides with unusual structural features and biological activities. The structure of 1 is composed of a [6,6] spiroketal core decorated with highly unsaturated side chains, As a prelude to the synthesis of 1, we present herein a short, efficient, and enantioselective synthesis of the C9-C21 fragment 5 (spiroketal core) of reveromycin A.

  DOI：

  10.1021/ol991290v

文献信息

• Organocatalytic Asymmetric Synthesis of 1,2,3-<i>prim</i>,<i>sec</i>,<i>sec</i>-Triols
  作者：Armando Córdova、Gui-Ling Zhao、Pawel Dziedzic、Ismail Ibrahem

  DOI：10.1055/s-2006-956488

  日期：2006.12

  A tandem organocatalytic asymmetric synthesis of 1,2,3-triols using a,b-unsaturated aldehydes as the substrates and hydrogen peroxide as the oxidant is presented. The reaction can also be applied to the asymmetric synthesis of 3-chloro-1,2-propandiols.

  本文介绍了以a,b-不饱和醛为底物、过氧化氢为氧化剂的串联有机催化的1,2,3-三醇不对称合成方法。此外，该反应亦可应用于3-氯-1,2-丙二醇的不对称合成。
• Enantioselective Synthesis of the [6,6] Spiroketal Core of Reveromycin A
  作者：Keith E. Drouet、Taotao Ling、Hung V. Tran、Emmanuel A. Theodorakis

  DOI：10.1021/ol991290v

  日期：2000.1.1

  Reveromycin A (1) belongs to a family of microbial polyketides with unusual structural features and biological activities. The structure of 1 is composed of a [6,6] spiroketal core decorated with highly unsaturated side chains, As a prelude to the synthesis of 1, we present herein a short, efficient, and enantioselective synthesis of the C9-C21 fragment 5 (spiroketal core) of reveromycin A.