[4S-4α,7β,9α,9aα]-1,6-dioxo-7-methyl-4-phenyloctahydropyrido[2,1-c][1,4]oxazine-9-carboxylic acid methyl ester | 181787-03-1

• 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: [4S-4α,7β,9α,9aα]-1,6-dioxo-7-methyl-4-phenyloctahydropyrido[2,1-c][1,4]oxazine-9-carboxylic acid methyl ester
• 英文别名: methyl (4S,7S,9S,9aR)-7-methyl-1,6-dioxo-4-phenyl-3,4,7,8,9,9a-hexahydropyrido[2,1-c][1,4]oxazine-9-carboxylate
• CAS: 181787-03-1
• 化学式: C₁₇H₁₉NO₅
• 分子量: 317.342
• InChiKey: ANDBMAKTFNPCHK-SCUASFONSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  72.9
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  [4S-4α,7β,9α,9aα]-1,6-dioxo-7-methyl-4-phenyloctahydropyrido[2,1-c][1,4]oxazine-9-carboxylic acid methyl ester 在 硼烷四氢呋喃络合物 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以85%的产率得到[4S-4α,7β,9α,9aα]-1-oxo-7-methyl-4-phenyloctahydropyrido[2,1-c][1,4]oxazine-9-carboxylic acid methyl ester
  参考文献：
  名称：

  Enantioselective Synthesis of Conformationally Restricted Analogs of NMDA:  cis- and trans-Piperidine-2,3-dicarboxylic Acids and Methylated Derivatives

  摘要：

  Various enantiopure stereoisomeric cyclic amino diacids belonging to the 2,3-piperidinedicarboxylic acid series mere obtained via an aza-annulation reaction between enamino esters and acryloyl, methacryloyl, or crotonyl chloride. Enantioselective syntheses of these conformationnally restricted analogs of N-methyl-D-aspartic acid were realized owing to a chiral induction originated from (2S)-2-phenylglycinol. New information about the mechanism of the aza-annulation process is inferred from AM1 calculations which were performed in order to explain the steroselectivity displayed during the formation of the C-4 stereocenter In compound 4.

  DOI：

  10.1021/jo9606158
• 作为产物：
  描述：

  L-苯甘氨醇 在 镍 氢气 作用下， 以 四氢呋喃 、 乙醇 、 乙酸乙酯 为溶剂， 反应 24.5h， 生成 [4S-4α,7β,9α,9aα]-1,6-dioxo-7-methyl-4-phenyloctahydropyrido[2,1-c][1,4]oxazine-9-carboxylic acid methyl ester
  参考文献：
  名称：

  Enantioselective Synthesis of Conformationally Restricted Analogs of NMDA:  cis- and trans-Piperidine-2,3-dicarboxylic Acids and Methylated Derivatives

  摘要：

  Various enantiopure stereoisomeric cyclic amino diacids belonging to the 2,3-piperidinedicarboxylic acid series mere obtained via an aza-annulation reaction between enamino esters and acryloyl, methacryloyl, or crotonyl chloride. Enantioselective syntheses of these conformationnally restricted analogs of N-methyl-D-aspartic acid were realized owing to a chiral induction originated from (2S)-2-phenylglycinol. New information about the mechanism of the aza-annulation process is inferred from AM1 calculations which were performed in order to explain the steroselectivity displayed during the formation of the C-4 stereocenter In compound 4.

  DOI：

  10.1021/jo9606158

文献信息

• Enantioselective Synthesis of Conformationally Restricted Analogs of NMDA:  <i>cis</i>- and <i>trans</i>-Piperidine-2,3-dicarboxylic Acids and Methylated Derivatives
  作者：Claude Agami、Louis Hamon、Catherine Kadouri-Puchot、Valérie Le Guen

  DOI：10.1021/jo9606158

  日期：1996.1.1

  Various enantiopure stereoisomeric cyclic amino diacids belonging to the 2,3-piperidinedicarboxylic acid series mere obtained via an aza-annulation reaction between enamino esters and acryloyl, methacryloyl, or crotonyl chloride. Enantioselective syntheses of these conformationnally restricted analogs of N-methyl-D-aspartic acid were realized owing to a chiral induction originated from (2S)-2-phenylglycinol. New information about the mechanism of the aza-annulation process is inferred from AM1 calculations which were performed in order to explain the steroselectivity displayed during the formation of the C-4 stereocenter In compound 4.