(1^IR,1^IIIS,3S,4^IIS,4^IVR,5R)-3,5-bis[(2,2-dimethyl-[1,3]dioxolan-4-yl)hydroxymethyl]-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester | 874343-13-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (1^IR,1^IIIS,3S,4^IIS,4^IVR,5R)-3,5-bis[(2,2-dimethyl-[1,3]dioxolan-4-yl)hydroxymethyl]-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester
• 英文别名: tert-butyl (3S,5R)-3-[(R)-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-hydroxymethyl]-5-[(S)-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-hydroxymethyl]-2-oxopyrrolidine-1-carboxylate
• CAS: 874343-13-2
• 化学式: C₂₁H₃₅NO₉
• 分子量: 445.51
• InChiKey: NEPJKLNVPXNYRG-PRFSMCDRSA-N

物化性质

• 沸点：
  584.3±35.0 °C(Predicted)
• 密度：
  1.236±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  124
• 氢给体数：
  2
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  (1^IR,1^IIIS,3S,4^IIS,4^IVR,5R)-3,5-bis[(2,2-dimethyl-[1,3]dioxolan-4-yl)hydroxymethyl]-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester 在 2,6-二甲基吡啶 、 盐酸 、 4-二甲氨基吡啶 、 samarium diiodide 、 ammonium cerium(IV) nitrate 、 高碘酸 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 乙酸乙酯 、 乙腈 为溶剂， 反应 26.0h， 生成 (1S,2S,3R,4R,5S,6R)-6-amino-2,3,4,5-tetrahydroxycycloheptanecarboxylic acid
  参考文献：
  名称：

  New Enantioselective Entry to Cycloheptane Amino Acid Polyols

  摘要：

  A diversity-oriented protocol has been developed for the assembly of densely hydroxylated cycloheptane amino acids via succession of a vinylogous Mukaiyama aldol reaction (VMAR), a Morita-Baylis-Hillman reaction (MBHR), and an intramolecular pinacol coupling reaction (IPCR). The plan utilizes Dor L-configured glyceraldehyde derivatives as "chiral" surrogates of glyoxal and N-[(tert-butoxycarbonyl)2-(tert-butyldimethylsilyl)oxy]pyrrole as the synthetic equivalent of the alpha,gamma-dianion of gamma-aminobutanoic acid. The parallel, asymmetric syntheses of four cycloheptane representatives proceed with high diastereocontrol and virtually complete enantioselectivity in ten steps and overall yields of 15-37%.

  DOI：

  10.1021/jo0520137
• 作为产物：
  描述：

  (R)-(+)-2,2-二甲基-1,3-二氧戊环-4-甲醛 在 palladium on activated charcoal 吡啶 、 正丁基锂 、 二苯基二硒醚 、 氢气 、 sodium acetate 、 四氯化锡 、 柠檬酸 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 9.0h， 生成 (1^IR,1^IIIS,3S,4^IIS,4^IVR,5R)-3,5-bis[(2,2-dimethyl-[1,3]dioxolan-4-yl)hydroxymethyl]-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  New Enantioselective Entry to Cycloheptane Amino Acid Polyols

  摘要：

  A diversity-oriented protocol has been developed for the assembly of densely hydroxylated cycloheptane amino acids via succession of a vinylogous Mukaiyama aldol reaction (VMAR), a Morita-Baylis-Hillman reaction (MBHR), and an intramolecular pinacol coupling reaction (IPCR). The plan utilizes Dor L-configured glyceraldehyde derivatives as "chiral" surrogates of glyoxal and N-[(tert-butoxycarbonyl)2-(tert-butyldimethylsilyl)oxy]pyrrole as the synthetic equivalent of the alpha,gamma-dianion of gamma-aminobutanoic acid. The parallel, asymmetric syntheses of four cycloheptane representatives proceed with high diastereocontrol and virtually complete enantioselectivity in ten steps and overall yields of 15-37%.

  DOI：

  10.1021/jo0520137

文献信息

• New Enantioselective Entry to Cycloheptane Amino Acid Polyols
  作者：Claudio Curti、Franca Zanardi、Lucia Battistini、Andrea Sartori、Gloria Rassu、Luciana Auzzas、Annamaria Roggio、Luigi Pinna、Giovanni Casiraghi

  DOI：10.1021/jo0520137

  日期：2006.1.1

  A diversity-oriented protocol has been developed for the assembly of densely hydroxylated cycloheptane amino acids via succession of a vinylogous Mukaiyama aldol reaction (VMAR), a Morita-Baylis-Hillman reaction (MBHR), and an intramolecular pinacol coupling reaction (IPCR). The plan utilizes Dor L-configured glyceraldehyde derivatives as "chiral" surrogates of glyoxal and N-[(tert-butoxycarbonyl)2-(tert-butyldimethylsilyl)oxy]pyrrole as the synthetic equivalent of the alpha,gamma-dianion of gamma-aminobutanoic acid. The parallel, asymmetric syntheses of four cycloheptane representatives proceed with high diastereocontrol and virtually complete enantioselectivity in ten steps and overall yields of 15-37%.