(2R,3S)-1-(tert-Butyloxycarbonyl)-3-<1-(3-cyanoindolyl)methyl>aziridine-2-carboxylic acid | 159763-76-5

• 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: (2R,3S)-1-(tert-Butyloxycarbonyl)-3-<1-(3-cyanoindolyl)methyl>aziridine-2-carboxylic acid
• 英文别名: (2R,3S)-3-[(3-cyanoindol-1-yl)methyl]-1-[(2-methylpropan-2-yl)oxycarbonyl]aziridine-2-carboxylic acid
• CAS: 159763-76-5
• 化学式: C₁₈H₁₉N₃O₄
• 分子量: 341.367
• InChiKey: QKRPQSXEAPAXEF-ZOMUKPOZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  25
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  95.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (2R,3S)-1-(tert-Butyloxycarbonyl)-3-<1-(3-cyanoindolyl)methyl>aziridine-2-carboxylic acid 在 三丁基膦 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 生成 tert-butyl N-[(2S)-1-(3-cyanoindol-1-yl)-3-oxopropan-2-yl]carbamate
  参考文献：
  名称：

  Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles

  摘要：

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.

  DOI：

  10.1021/jo00105a009
• 作为产物：
  描述：

  3-氰基吲哚 在 lithium hydroxide 、 sodium hexamethyldisilazane 作用下， 以 四氢呋喃 为溶剂， 反应 5.0h， 生成 (2R,3S)-1-(tert-Butyloxycarbonyl)-3-<1-(3-cyanoindolyl)methyl>aziridine-2-carboxylic acid
  参考文献：
  名称：

  Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles

  摘要：

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.

  DOI：

  10.1021/jo00105a009

文献信息

• Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles
  作者：Frederick E. Ziegler、Makonen Belema

  DOI：10.1021/jo00105a009

  日期：1994.12

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.