(S)-3-(but-3-enyl)carvone | 853562-45-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (S)-3-(but-3-enyl)carvone
• 英文别名: (5S)-3-(But-3-en-1-yl)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one；(5S)-3-but-3-enyl-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one
• CAS: 853562-45-5
• 化学式: C₁₄H₂₀O
• 分子量: 204.312
• InChiKey: CHQYWEBNWCDWGJ-ZDUSSCGKSA-N

物化性质

• 沸点：
  295.9±40.0 °C(Predicted)
• 密度：
  0.914±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  15
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (S)-3-(but-3-enyl)carvone 在 palladium dichloride sodium hydroxide 、 lithium aluminium tetrahydride 、 amberlyst-15 、 水 、 双氧水 、 氧气 、 对甲苯磺酸 、 copper(l) chloride 作用下， 以 甲醇 、 乙醚 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 苯 为溶剂， 反应 65.75h， 生成 (1S,2R,4S)-4-Isopropenyl-2-(2-methyl-[1,3]dioxolan-2-yl)-2-[2-(2-methyl-[1,3]dioxolan-2-yl)-ethyl]-cyclopentanol
  参考文献：
  名称：

  Enantiospecific total synthesis of phytoalexins, (+)-solanascone, (+)-dehydrosolanascone, and (+)-anhydro-β-rotunol

  摘要：

  Enantiospecific total synthesis of the phytoalexins, solavetivone, anhydro-beta-rotunol, solailascone, and dehydrosolanascone, starting from the readily available monoterpene, (R)-carvone has been accomplished. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.08.124
• 作为产物：
  描述：

  在 silica gel 、 pyridinium chlorochromate 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 生成 (S)-3-(but-3-enyl)carvone
  参考文献：
  名称：

  Enantiospecific first total synthesis of (+)-2β-hydroxysolanascone, the aglycone of the phytoalexin isolated from flue-cured tobacco leaves

  摘要：

  The first total synthesis of (+)-2 beta-hydroxysolanascone, the aglycone of the phytoalexin 2 beta-hydroxysolanascone-beta-glucopyranoside isolated from flue-cured tobacco leaves (N. tabacian L., OCL), and its 2,10-diepi- and 2 alpha-epimers has been accomplished, starting from the readily available monoterpene (R)-carvone. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2005.11.014

文献信息

• Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular carbonyl ene-reaction
  作者：A. Srikrishna、C. Dinesh、K. Anebouselvy

  DOI：10.1016/s0040-4039(98)02518-0

  日期：1999.1

  Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular acid catalysed type II ene reaction of chiral (5-isopropenylcyclohex-2-enyl)acetaldehydes derived from (R)-carvone is described.

  描述了通过分子内酸催化衍生自（R）-香芹酮的手性（5-异丙烯基环己-2-烯基）乙醛的II型烯反应合成手性双环[4.3.1]癸烷。
• Enantiospecific total synthesis of phytoalexins, (+)-solanascone, (+)-dehydrosolanascone, and (+)-anhydro-β-rotunol
  作者：A. Srikrishna、S.S.V. Ramasastry

  DOI：10.1016/j.tetlet.2005.08.124

  日期：2005.10

  Enantiospecific total synthesis of the phytoalexins, solavetivone, anhydro-beta-rotunol, solailascone, and dehydrosolanascone, starting from the readily available monoterpene, (R)-carvone has been accomplished. (c) 2005 Elsevier Ltd. All rights reserved.
• An efficient construction of a C3-symmetric macrocycle by head to tail cyclotrimerization of an unsymmetrical diene via a sequence of highly regio- and stereoselective metathesis reactions
  作者：A. Srikrishna、Dattatraya H. Dethe

  DOI：10.1016/j.tetlet.2005.03.088

  日期：2005.5

  A sequence of highly regio- and stereoselective intermolecular metatheses followed by ring-closing metathesis of an 1-allyl-3-(3-butenyl)cyclohexanol led to a C-3-symmetric head to tail cyclic trimer; a 24-membered macrocycle containing three inward directed hydroxyl groups creating a hydrophilic cavity. (c) 2005 Elsevier Ltd. All rights reserved.
• Enantiospecific first total synthesis of (+)-2β-hydroxysolanascone, the aglycone of the phytoalexin isolated from flue-cured tobacco leaves
  作者：A. Srikrishna、S.S.V. Ramasastry

  DOI：10.1016/j.tetlet.2005.11.014

  日期：2006.1

  The first total synthesis of (+)-2 beta-hydroxysolanascone, the aglycone of the phytoalexin 2 beta-hydroxysolanascone-beta-glucopyranoside isolated from flue-cured tobacco leaves (N. tabacian L., OCL), and its 2,10-diepi- and 2 alpha-epimers has been accomplished, starting from the readily available monoterpene (R)-carvone. (c) 2005 Elsevier Ltd. All rights reserved.