(S)-5-Hydroxy-cyclohexa-1,3-dienecarboxylic acid tert-butyl ester | 191795-30-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-5-Hydroxy-cyclohexa-1,3-dienecarboxylic acid tert-butyl ester
• 英文别名: tert-butyl (5S)-5-hydroxycyclohexa-1,3-diene-1-carboxylate
• CAS: 191795-30-9
• 化学式: C₁₁H₁₆O₃
• 分子量: 196.246
• InChiKey: FWXCGPVQHGJNAV-SECBINFHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-5-Hydroxy-cyclohexa-1,3-dienecarboxylic acid tert-butyl ester 在 四氧化锇 、 十二/十四烷基二甲基氧化胺 、 2,6-futidine 、 三氟乙酸 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 0.25h， 生成 (+)-莽草酸
  参考文献：
  名称：

  Enantioselective synthesis of (+)-shikimic acid and (+)-5-epi-shikimic acid by asymmetric Diels-Alder reaction of (S)-α-sulfinylacrylates

  摘要：

  Enantiopure (S) benzyl and t-butyl 2-p-tolylsulfinylpropenoates (1 and 2) were readily prepared by Mannich condensation of (R) p-tolylsulfinylacetates (CH2O+Me2NH), followed by in situ nitrogen quaternization. These new chiral dienophiles reacted with furan at high pressures (4-13 Kbar) at rt to afford mainly a 2:1 mixture of both endo adducts (endo-B+endo-A). Enantiopure endo-4B and endo-4A were stereoselectively transformed into (+)-shikimic acid and (+)-5-epi-shikimic acid respectively, by dihydroxylation of the double bond, removal of the sulfinyl group, basic opening of the oxabicyclic skeleton and hydrolysis of the ester moiety. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(97)00151-1
• 作为产物：
  描述：

  7-Oxa-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid tert-butyl ester 在 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 为溶剂， 以94%的产率得到(S)-5-Hydroxy-cyclohexa-1,3-dienecarboxylic acid tert-butyl ester
  参考文献：
  名称：

  Enantioselective synthesis of (+)-shikimic acid and (+)-5-epi-shikimic acid by asymmetric Diels-Alder reaction of (S)-α-sulfinylacrylates

  摘要：

  Enantiopure (S) benzyl and t-butyl 2-p-tolylsulfinylpropenoates (1 and 2) were readily prepared by Mannich condensation of (R) p-tolylsulfinylacetates (CH2O+Me2NH), followed by in situ nitrogen quaternization. These new chiral dienophiles reacted with furan at high pressures (4-13 Kbar) at rt to afford mainly a 2:1 mixture of both endo adducts (endo-B+endo-A). Enantiopure endo-4B and endo-4A were stereoselectively transformed into (+)-shikimic acid and (+)-5-epi-shikimic acid respectively, by dihydroxylation of the double bond, removal of the sulfinyl group, basic opening of the oxabicyclic skeleton and hydrolysis of the ester moiety. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0957-4166(97)00151-1

文献信息

• Enantioselective synthesis of (+)-shikimic acid and (+)-5-epi-shikimic acid by asymmetric Diels-Alder reaction of (S)-α-sulfinylacrylates
  作者：Javier Adrio、Juan C. Carretero、Jose L. García Ruano、Luisa M. Martín Cabrejas

  DOI：10.1016/s0957-4166(97)00151-1

  日期：1997.5

  Enantiopure (S) benzyl and t-butyl 2-p-tolylsulfinylpropenoates (1 and 2) were readily prepared by Mannich condensation of (R) p-tolylsulfinylacetates (CH2O+Me2NH), followed by in situ nitrogen quaternization. These new chiral dienophiles reacted with furan at high pressures (4-13 Kbar) at rt to afford mainly a 2:1 mixture of both endo adducts (endo-B+endo-A). Enantiopure endo-4B and endo-4A were stereoselectively transformed into (+)-shikimic acid and (+)-5-epi-shikimic acid respectively, by dihydroxylation of the double bond, removal of the sulfinyl group, basic opening of the oxabicyclic skeleton and hydrolysis of the ester moiety. (C) 1997 Elsevier Science Ltd.