(2S)-1-(cyclohex-1-en-1-yl)pent-4-en-2-ol | 399513-61-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S)-1-(cyclohex-1-en-1-yl)pent-4-en-2-ol
• 英文别名: (2S)-1-cyclohex-1-enyl-pent-4-en-2-ol；(2S)-1-(cyclohexen-1-yl)pent-4-en-2-ol
• CAS: 399513-61-2
• 化学式: C₁₁H₁₈O
• 分子量: 166.263
• InChiKey: FXBUZGDHYCXKPU-NSHDSACASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  12
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (2S)-1-(cyclohex-1-en-1-yl)pent-4-en-2-ol 、 对硝基苯甲酸 在 4-二甲氨基吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 16.0h， 以71%的产率得到4-nitrobenzoic acid (2S)-1-(cyclohex-1-enyl)methylbut-3-enyl ester
  参考文献：
  名称：

  Enantioselective Allylation and Crotylation of in situ Generated β,γ-Unsaturated Aldehydes

  摘要：

  用催化量的 Sc(OTf)3 处理 2-乙烯基环氧乙烷原位生成的 β,γ-不饱和醛被环应变烯丙基和巴豆基硅烷试剂有效捕获，以高对映体过量的形式提供双烯丙基醇作为单一非对映体。

  DOI：

  10.1055/s-0031-1289565
• 作为产物：
  描述：

  (+/-)-(2E)-2-cyclohex-1-enyl-oxirane 、 (+)-Ipc2B(烯丙基)硼烷 在 scandium tris(trifluoromethanesulfonate) 作用下， 以 四氢呋喃 为溶剂， 反应 40.0h， 以92%的产率得到(2S)-1-(cyclohex-1-en-1-yl)pent-4-en-2-ol
  参考文献：
  名称：

  Chemoselective Cross Metathesis of Bishomoallylic Alcohols:  Rapid Access to Fragment A of the Cryptophycins

  摘要：

  The racemic or enantioselective allylation of in situ formed beta,gamma-unsaturated aldehydes provides efficient access to bishomoallylic alcohols from readily available 2-vinyloxiranes. These products, when subjected to modified Grubbs cross metathesis conditions, afforded terminally homologated products in moderate to good yields with high E selectivity and without degradation of the enantiomeric excess. The compounds obtained through this two-step sequence yield fragments of an important and pharmacologically active family of cryptophycins.

  DOI：

  10.1021/ol049883f

文献信息

• Enantioselective Allylation of <i>β</i><i>,</i><i>γ</i>-Unsaturated Aldehydes Generated via Lewis Acid Induced Rearrangement of 2-Vinyloxiranes
  作者：Mark Lautens、Matthew L. Maddess、Effiette L. O. Sauer、Stéphane G. Ouellet

  DOI：10.1021/ol016946a

  日期：2002.1.1

  [reaction: see text] 2-Vinyloxiranes have been found to be excellent surrogates to beta,gamma-unsaturated aldehydes. These valuable electrophiles, generated in situ by treatment of a 2-vinyloxirane with a catalytic amount of Sc(OTf)(3), are effectively trapped by the chiral allylating agents based on alpha-pinene, affording bishomoallylic alcohols in high yield and excellent selectivity.

  [反应：见正文]已发现2-乙烯基氧杂环戊烷是β，γ-不饱和醛的优良替代物。这些有价值的亲电试剂是通过催化量的Sc（OTf）（3）处理2-乙烯基环氧乙烷而原位生成的，它们被基于α-pine烯的手性烯丙基化剂有效地捕获，从而以高收率和优异的选择性提供了双烯丙基烯丙醇。 。
• Chemoselective Cross Metathesis of Bishomoallylic Alcohols:  Rapid Access to Fragment A of the Cryptophycins
  作者：Mark Lautens、Matthew L. Maddess

  DOI：10.1021/ol049883f

  日期：2004.6.1

  The racemic or enantioselective allylation of in situ formed beta,gamma-unsaturated aldehydes provides efficient access to bishomoallylic alcohols from readily available 2-vinyloxiranes. These products, when subjected to modified Grubbs cross metathesis conditions, afforded terminally homologated products in moderate to good yields with high E selectivity and without degradation of the enantiomeric excess. The compounds obtained through this two-step sequence yield fragments of an important and pharmacologically active family of cryptophycins.
• Enantioselective Allylation and Crotylation of in situ Generated β,γ-Unsaturated Aldehydes
  作者：Mark Lautens、J. McCubbin、Matthew Maddess

  DOI：10.1055/s-0031-1289565

  日期：2011.12

  β,γ-Unsaturated aldehydes generated in situ by treatment of 2-vinyloxiranes with a catalytic amount of Sc(OTf)3 are effectively trapped by ring-strained allyl- and crotylsilane reagents to afford bishomoallylic alcohols as single diastereomers in high enantiomeric excess.

  用催化量的 Sc(OTf)3 处理 2-乙烯基环氧乙烷原位生成的 β,γ-不饱和醛被环应变烯丙基和巴豆基硅烷试剂有效捕获，以高对映体过量的形式提供双烯丙基醇作为单一非对映体。