3-((3aR,4R,6R,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-propan-1-ol | 132375-60-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氧吡喃
• 英文名称: 3-((3aR,4R,6R,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-propan-1-ol
• 英文别名: 3-[(3aR,4R,6R,7aS)-2,2-dimethyl-4-prop-2-enyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-6-yl]propan-1-ol
• CAS: 132375-60-1
• 化学式: C₁₄H₂₄O₄
• 分子量: 256.342
• InChiKey: AIUVDBCMOUVTIA-FVCCEPFGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  47.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-((3aR,4R,6R,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-propan-1-ol 以95%的产率得到
  参考文献：
  名称：

  NICOLAOU, K. C.;VEALE, C. A.;HWANG, C. -K.;HUTCHINSON, J.;PRASAD, C. V. C+, ANGEW. CHEM., 103,(1991) N, C. 304-308

  摘要：

  DOI：
• 作为产物：
  描述：

  3-((3aR,4R,6R,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-propionic acid methyl ester 在 二异丁基氢化铝 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 3-((3aR,4R,6R,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-propan-1-ol
  参考文献：
  名称：

  Nicolaou, K. C.; Veale, C. A.; Hwang, C.-K., Angewandte Chemie, 1991, vol. 103, # 3, p. 304 - 308

  摘要：

  DOI：

文献信息

• Stereocontrolled Total Synthesis of Hemibrevetoxin B
  作者：Isao Kadota、Yoshinori Yamamoto

  DOI：10.1021/jo9807619

  日期：1998.9.1

  The stereocontrolled total synthesis of hemibrevetoxin B (1) has been achieved in 56 steps and 0.75% overall yield from D-mannose. The intramolecular reaction of gamma-alkoxyallylstannane with. aldehyde is a key step for the present total synthesis. Thus, the BF3. OEt2-mediated reaction of 24 gave 6 as a sole product. We encountered difficulty in the synthesis of gamma-alkoxyallylstannane 30 from the corresponding allyl ether 29 in which the gamma-alkoxy substituent became sterically quite bulky. This problem was solved by developing the acetal cleavage method for the synthesis of gamma-alkoxyallylstannanes. The cyclization of 38 proceeded smoothly to give the key intermediate 5 in a highly stereoselective manner. Construction of the alpha-vinyl aldehyde and (Z)-diene moieties were performed using Nicolaou's protocol.
• Total Synthesis of Hemibrevetoxin B
  作者：I Kadota

  DOI：10.1016/00404-0399(50)10972-

  日期：1995.8.7

  The total synthesis of Hemibrevetoxin B is described. A new cyclization approach, based on the Lewis acid mediated intramolecular cyclization of the gamma-oxo-substituted allylic tin having an aldehyde group, produced the 6-6-7-7 polycyclic ether skeleton of the natural product with high stereoselectivity. The H-1 and C-13-NMR spectra of synthetic hemibrevetoxin B was identical with those of natural product.
• NICOLAOU, K. C.;VEALE, C. A.;HWANG, C. -K.;HUTCHINSON, J.;PRASAD, C. V. C+, ANGEW. CHEM., 103,(1991) N, C. 304-308
  作者：NICOLAOU, K. C.、VEALE, C. A.、HWANG, C. -K.、HUTCHINSON, J.、PRASAD, C. V. C+

  DOI：——

  日期：——
• Nicolaou, K. C.; Veale, C. A.; Hwang, C.-K., Angewandte Chemie, 1991, vol. 103, # 3, p. 304 - 308
  作者：Nicolaou, K. C.、Veale, C. A.、Hwang, C.-K.、Hutchinson, J.、Prasad, C. V. C.、Ogilvie, W. W.

  DOI：——

  日期：——