(S)-(-)-dodec-2-en-4-ol | 139559-27-6

• 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)-(-)-dodec-2-en-4-ol
• CAS: 139559-27-6
• 化学式: C₁₂H₂₄O
• 分子量: 184.322
• InChiKey: BJCSERFEWVMCMW-LHJMJDNXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.67
• 重原子数：
  13.0
• 可旋转键数：
  8.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  20.23
• 氢给体数：
  1.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  (S)-(-)-dodec-2-en-4-ol 在 吡啶 、 4-二甲氨基吡啶 、 二甲基硫 、 臭氧 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成
  参考文献：
  名称：

  Catalytic asymmetric synthesis of protected α-hydroxy aldehydes and related 1,2-difunctional chiral building blocks. An enantioselective synthesis of (−)-exo- and (−)-endo-brevicomin

  摘要：

  Chiral allylic alcohols which were prepared by the addition of functionalized dialkylzincs to alpha,beta-unsaturated aldehydes in good to excellent enantioselectivity, were converted to protected alpha-hydroxy aldehydes and 1,2-amino alcohols without loss of enantiomeric purity. Syn- or anti-1,2-diols can be obtained stereoselectively by a second asymmetric addition to alpha-silyloxy aldehydes. Functionalized 1,2-diols prepared in this way were converted to enantiomerically pure (-)-exo- and (-)-endo-brevicomin (>99% ee). (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(97)00036-0
• 作为产物：
  描述：

  dodec-2-en-4-ol 生成 (S)-(-)-dodec-2-en-4-ol 、 (R)-(+)-dodec-2-en-4-ol
  参考文献：
  名称：

  Highly stereoselective allylic ethylation with alkoxytitanacyclopropane reagents. Synthesis of (1R/S,7R)-1,7-dimethylnonyl propanoate, the Western corn rootworm sex attractant

  摘要：

  Allylic ethylation of 2-((E)-dodec-2-en-4-yloxy)tetrahydro-2H-pyran with ethylmagnesium bromide in the presence of titanium(IV) isopropoxide proceeds Via a S(N)2' pathway to afford (E)-3-methyltridec-4-ene with excellent syn-diastereoselecivity. This transformation is used as a key step in the synthesis of (1R/S,7R)- 1,7-dimethylnonyl propanoate, the Western corn rootworm (Diabrotica virgifera virgifera) sex attractant. (C) 2008 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tetlet.2008.08.063

文献信息

• Synthesis of ethisolide, isoavenaciolide, and avenaciolide
  作者：Steven D. Burke、Gregory J. Pacofsky、Anthony D. Piscopio

  DOI：10.1021/jo00034a009

  日期：1992.4

  Syntheses of the trio of related mold metabolites ethisolide (1), isoavenaciolide (2), and avenaciolide (3) in racemic and optically active forms are described. Glycolate Claisen rearrangements governed by chelation control of enolate geometry and diastereofacial bias in the [3,3] shifts establish the functional and stereochemical details in butyrolactone precursors (15b, 22, and 19) of the natural products. Lactone rearrangements via complementary bis(transesterification) (22 --> 23) and carboxylate displacement/lactonization (26 --> 27 --> 3) reactions provided the diastereomeric isoavenaciolide and avenaciolide structures. Differential reactivities among potential transacylation substrates 15a, 15b, 21, 22, 24, and 26 are attributed to steric interactions or strain in bridged bicyclic intermediates 32, 34, and 36.
• Catalytic asymmetric synthesis of protected α-hydroxy aldehydes and related 1,2-difunctional chiral building blocks. An enantioselective synthesis of (−)-exo- and (−)-endo-brevicomin
  作者：S. Vettel、C. Lutz、A. Diefenbach、G. Haderlein、S. Hammerschmidt、K. Kühling、M.-R. Mofid、T. Zimmermann、P. Knochel

  DOI：10.1016/s0957-4166(97)00036-0

  日期：1997.3

  Chiral allylic alcohols which were prepared by the addition of functionalized dialkylzincs to alpha,beta-unsaturated aldehydes in good to excellent enantioselectivity, were converted to protected alpha-hydroxy aldehydes and 1,2-amino alcohols without loss of enantiomeric purity. Syn- or anti-1,2-diols can be obtained stereoselectively by a second asymmetric addition to alpha-silyloxy aldehydes. Functionalized 1,2-diols prepared in this way were converted to enantiomerically pure (-)-exo- and (-)-endo-brevicomin (>99% ee). (C) 1997 Elsevier Science Ltd.
• Highly stereoselective allylic ethylation with alkoxytitanacyclopropane reagents. Synthesis of (1R/S,7R)-1,7-dimethylnonyl propanoate, the Western corn rootworm sex attractant
  作者：Vladimir E. Isakov、Oleg G. Kulinkovich

  DOI：10.1016/j.tetlet.2008.08.063

  日期：2008.12

  Allylic ethylation of 2-((E)-dodec-2-en-4-yloxy)tetrahydro-2H-pyran with ethylmagnesium bromide in the presence of titanium(IV) isopropoxide proceeds Via a S(N)2' pathway to afford (E)-3-methyltridec-4-ene with excellent syn-diastereoselecivity. This transformation is used as a key step in the synthesis of (1R/S,7R)- 1,7-dimethylnonyl propanoate, the Western corn rootworm (Diabrotica virgifera virgifera) sex attractant. (C) 2008 Published by Elsevier Ltd.