(1S,2S,6S)-(+)-(2-Hydroxy-2,6-dimethyl-6-vinylcyclohexyl)acetic acid | 104640-78-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1S,2S,6S)-(+)-(2-Hydroxy-2,6-dimethyl-6-vinylcyclohexyl)acetic acid
• 英文别名: (1S,2S,6S)-2-(2-hydroxy-2,6-dimethyl-6-vinylcyclohexanyl)acetic acid；2-[(1S,2S,6S)-2-ethenyl-6-hydroxy-2,6-dimethylcyclohexyl]acetic acid
• CAS: 104640-78-0
• 化学式: C₁₂H₂₀O₃
• 分子量: 212.289
• InChiKey: MKKFTMMPINDCQH-WCQGTBRESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  57.5
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1S,2S,6S)-(+)-(2-Hydroxy-2,6-dimethyl-6-vinylcyclohexyl)acetic acid 在 2-氯-1-甲基吡啶碘化物 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 12.0h， 生成 (3aS,4S,7aS)-(-)-Epianastrephin
  参考文献：
  名称：

  Mori, Kenji; Nakazono, Yutaka, Liebigs Annalen der Chemie, 1988, p. 167 - 174

  摘要：

  DOI：
• 作为产物：
  描述：

  (±)-epianastrephin 在 2-羟基吡啶 、 sodium hydroxide 作用下， 以 乙醇 、 甲苯 为溶剂， 反应 48.0h， 生成 (1S,2S,6S)-(+)-(2-Hydroxy-2,6-dimethyl-6-vinylcyclohexyl)acetic acid
  参考文献：
  名称：

  Resolution and assignment of absolute configuration to the enantiomers of anastrephin and epianastrephin and their analogs

  摘要：

  DOI：

  10.1021/jo00375a016

文献信息

• Diastereoselective Synthesis of (±)-Epianastrephin, (±)-Anastrephin and Analogs Thereof
  申请人：The United States of America, as Represented by the Secretary of Agriculture

  公开号：US20170305874A1

  公开（公告）日：2017-10-26

  A process for the synthesis of trans-fused γ-lactones having Formula (IV) from substituted cyclic ketones having Formula (I). A diastereoselective synthesis of (±)-epianastrephin (1) (wherein: R 1 is ethenyl, R 2 and R 3 is methyl, and n is 1), (±)-anastrephin (2) (wherein: R 2 is ethenyl, R 1 and R 3 is methyl and n is 1), and analogs thereof (wherein: R 1 is H, C 1-5 alkyl, C 2-6 alkenyl or C 2-6 alkynyl, R 2 is H, C 1-5 alkyl, C 2-6 alkenyl or C 2-6 alkynyl, R 1 and R 2 together with the carbon atom they are attached form a C 3-6 cycloalkyl ring, R 3 is C 1-5 alkyl and n is 0-2):

  从具有化学式（I）的取代环状酮合成具有化学式（IV）的反式γ-内酯的过程。对（±）-epianastrephin（1）进行立体选择合成（其中：R1为乙烯基，R2和R3为甲基，n为1），（±）-anastrephin（2）进行立体选择合成（其中：R2为乙烯基，R1和R3为甲基，n为1），以及它们的类似物（其中：R1为H，C1-5烷基，C2-6烯基或C2-6炔基，R2为H，C1-5烷基，C2-6烯基或C2-6炔基，R1和R2与它们附着的碳原子一起形成C3-6环烷基环，R3为C1-5烷基，n为0-2）。
• Diastereoselective synthesis of (±)-epianastrephin, (±)-anastrephin and analogs thereof
  申请人：The United States of America, as Represented by the Secretary of Agriculture

  公开号：US10011580B2

  公开（公告）日：2018-07-03

  A process for the synthesis of trans-fused γ-lactones having Formula (IV) from substituted cyclic ketones having Formula (I). A diastereoselective synthesis of (±)-epianastrephin (1) (wherein: R1 is ethenyl, R2 and R3 is methyl, and n is 1), (±)-anastrephin (2) (wherein: R2 is ethenyl, R1 and R3 is methyl and n is 1), and analogs thereof (wherein: R1 is H, C1-5 alkyl, C2-6 alkenyl or C2-6 alkynyl, R2 is H, C1-5 alkyl, C2-6 alkenyl or C2-6 alkynyl, R1 and R2 together with the carbon atom they are attached form a C3-6 cycloalkyl ring, R3 is C1-5 alkyl and n is 0-2):

  一种从具有式(I)的取代环酮合成具有式(IV)的反式融合γ-内酯的工艺。一种非对映选择性合成(±)-epianastrephin (1)（其中：R1 是乙烯基，R2 和 R3 是甲基，n 是 1）、(±)-anastrephin (2)（其中：R2 是乙烯基，R1 和 R3 是甲基，n 是 1）及其类似物（其中：R1为H、C1-5烷基、C2-6烯基或C2-6炔基，R2为H、C1-5烷基、C2-6烯基或C2-6炔基，R1和R2与它们所连接的碳原子一起形成一个C3-6环烷基环，R3为C1-5烷基，n为0-2）：
• MORI, KENJI;NAKAZONO, YUTAKA, LIEBIGS ANN. CHEM.,(1988) N 2, 167-174
  作者：MORI, KENJI、NAKAZONO, YUTAKA

  DOI：——

  日期：——
• Glucosylated Suspensosides, Water-Soluble Pheromone Conjugates from the Oral Secretions of Male <i>Anastrepha suspensa</i>
  作者：Spencer S. Walse、Fang Lu、Peter E. A. Teal

  DOI：10.1021/np800096k

  日期：2008.10.24

  A diastereomeric mixture of the glycosylated pheromones (6R)- (1a) and (6S)-beta-D-glucopyranosyl 2-(2,6-dimethyl-6-vinylcyclohex-1-enyl)acetate (1b), which we named respectively suspensoside A and suspensoside B. was isolated from the oral secretions of male Caribbean fruit flies, Anastrepha suspensa. The absolute stereochemical configurations were established using microsample NMR instrumentation, chiral gas chromatography, and chemical synthesis utilizing pure enantiomers of anastrephin, (3aS,4R,7aS)- (4a) or (3aR,4S,7aR)-4,7a-dimethyl-4-vinylhexahydrobenzofuran-2(3H)one (4b), its the aglycon precursor.