Z-D-Phe-Ser-OMe | 63655-58-3

• 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: Z-D-Phe-Ser-OMe
• 英文别名: methyl (2S)-3-hydroxy-2-[[(2R)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoyl]amino]propanoate
• CAS: 63655-58-3
• 化学式: C₂₁H₂₄N₂O₆
• 分子量: 400.431
• InChiKey: QWRVHVAOTRUOLA-MSOLQXFVSA-N

物化性质

• 沸点：
  667.9±55.0 °C(Predicted)
• 密度：
  1.257±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  29
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  114
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  Z-D-Phe-Ser-OMe 在 palladium on activated charcoal 咪唑 、 氢气 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 生成 Cbz-Ser(TBDMS)-D-Phe-Ser(TBDMS)-OMe
  参考文献：
  名称：

  Total Synthesis and Assignment of Configuration of Lissoclinamide 7

  摘要：

  The first total synthesis of lissoclinamide 7, a 21-membered cyclopeptide isolated from Lissoclinum bistratum, was accomplished in 23 steps and 4.4% overall yield. The extraordinary configurational lability of the thiazoline segments was overcome by a novel strategy combining the use of the Burgess reagent for multiple simultaneous oxazoline and thiazoline formations and an efficient oxazoline --> thiazoline heterocycle interconversion. In addition to the total synthesis, this work highlights the scope of alternative strategies toward Lissoclinum peptides and presents the preparation of analogues for SAR studies of the cytotoxic effects of this family of marine natural products.

  DOI：

  10.1021/ja962859f
• 作为产物：
  描述：

  N-苄氧羰基-D-苯丙氨酸 在 N-甲基吗啉 作用下， 以 二氯甲烷 为溶剂， 反应 0.25h， 生成 Z-D-Phe-Ser-OMe
  参考文献：
  名称：

  Total Synthesis and Assignment of Configuration of Lissoclinamide 7

  摘要：

  The first total synthesis of lissoclinamide 7, a 21-membered cyclopeptide isolated from Lissoclinum bistratum, was accomplished in 23 steps and 4.4% overall yield. The extraordinary configurational lability of the thiazoline segments was overcome by a novel strategy combining the use of the Burgess reagent for multiple simultaneous oxazoline and thiazoline formations and an efficient oxazoline --> thiazoline heterocycle interconversion. In addition to the total synthesis, this work highlights the scope of alternative strategies toward Lissoclinum peptides and presents the preparation of analogues for SAR studies of the cytotoxic effects of this family of marine natural products.

  DOI：

  10.1021/ja962859f

文献信息

• Studies on Hydroxy Amino Acids. VI. Formation of the Oxazoline Derivatives from<i>N</i>-Acyl-β-hydroxy Amino Acid Peptides
  作者：Kiichiro Nakajima、Haruki Kawai、Michihiro Takai、Kenji Okawa

  DOI：10.1246/bcsj.50.917

  日期：1977.4

  Oxazoline derivatives were mainly obtained from the O-tosyl-N-acyl-β-hydroxy amino acid peptides by β-elimination reaction. Dehydroalanine or hydantoin derivatives were isolated when the urethane type acyl groups were used.

  噁唑啉衍生物主要是从 O-对甲苯磺酰基-N-酰基-β-羟基氨基酸肽中β-消除反应得到的。当使用氨基甲酸酯型酰基时，可分离出脱羟基丙氨酸或海因衍生物。
• Total Synthesis and Assignment of Configuration of Lissoclinamide 7
  作者：Peter Wipf、Paul C. Fritch

  DOI：10.1021/ja962859f

  日期：1996.1.1

  The first total synthesis of lissoclinamide 7, a 21-membered cyclopeptide isolated from Lissoclinum bistratum, was accomplished in 23 steps and 4.4% overall yield. The extraordinary configurational lability of the thiazoline segments was overcome by a novel strategy combining the use of the Burgess reagent for multiple simultaneous oxazoline and thiazoline formations and an efficient oxazoline --> thiazoline heterocycle interconversion. In addition to the total synthesis, this work highlights the scope of alternative strategies toward Lissoclinum peptides and presents the preparation of analogues for SAR studies of the cytotoxic effects of this family of marine natural products.