(S)-5-<(tert-Butoxycarbonyl)amino>-6-phenyl-(E)-3-hexen-1-ol | 155099-11-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (S)-5-<(tert-Butoxycarbonyl)amino>-6-phenyl-(E)-3-hexen-1-ol
• 英文别名: tert-butyl N-[(E,2S)-6-hydroxy-1-phenylhex-3-en-2-yl]carbamate
• CAS: 155099-11-9
• 化学式: C₁₇H₂₅NO₃
• 分子量: 291.39
• InChiKey: MPIJINCLOGCOQH-XKOZXHHJSA-N

物化性质

• 沸点：
  447.2±45.0 °C(Predicted)
• 密度：
  1.060±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-5-<(tert-Butoxycarbonyl)amino>-6-phenyl-(E)-3-hexen-1-ol 在 jones' reagent 、 potassium carbonate 作用下， 以 丙酮 为溶剂， 反应 0.5h， 生成 Methyl (S)-5-<(tert-butoxycarbonyl)amino>-6-phenyl-(E)-3-hexenoate
  参考文献：
  名称：

  Stereoselective Epoxidation of Phe-Gly and Phe-Phe Vinyl Isosteres

  摘要：

  Novel Phe-Gly and Phe-Phe isosteres have been synthesized. Vinylic isosteres of Phe-Gly and Phe-Phe were prepared by facile Julia reactions, and the resulting stereoisomers were isolated and epoxidized (m-chloroperbenzoic acid). Observed stereoselectivities of epoxidation appear to emanate from a cooperative coordination of the incoming peracid by the carbamate group and the more weakly coordinating allylic ester function.

  DOI：

  10.1021/jo00084a037
• 作为产物：
  描述：

  BOC-PHE-甲氧基甲胺 在 sodium hydroxide 、 sodium tetrahydroborate 、 9-borabicyclo[3.3.1]nonane dimer 、 乙醚 、 potassium tert-butylate 、 双氧水 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 12.0h， 生成 (S)-5-<(tert-Butoxycarbonyl)amino>-6-phenyl-(E)-3-hexen-1-ol
  参考文献：
  名称：

  Phe-Gly E-链烯二肽等排物的新型合成

  摘要：

  对的Boc-PHE的合成的新策略ψ（Ë -CHCH）GlyOH（11）进行说明。通过β消除6的甲磺酰氧基生成双键。事实证明，这种消除是合成过程中的关键步骤。根据碱以及反应条件获得不同的产物。使用KO t Bu导致E-（5 S）-（叔丁氧羰基氨基）-6-苯基-1,3-己二烯7，而NaOMe导致γ消除，导致氮丙啶9。二烯7转化为相应的Pheψ（E-CH = CH）Gly等排烷烃，随后进行硼氢化和琼斯氧化反应。

  DOI：

  10.1016/0040-4039(96)01108-2

文献信息

• Peracid dependent stereoselectivity and functional group contribution to the stereocontrol of epoxidation of (E)-alkene dipeptide isosteres
  作者：Daniel Wiktelius、Wei Berts、Annika Jenmalm Jensen、Joachim Gullbo、Stina Saitton、Ingeborg Csöregh、Kristina Luthman

  DOI：10.1016/j.tet.2006.01.095

  日期：2006.4

  on epoxidations with m-CPBA. The alkenes were synthesised in high yields with high E/Z-selectivities using either the Julia or Schlosser reactions. The formation of threo isomers was favoured in all epoxidation reactions except with CF3CO3H on substrates containing two allylic/homoallylic functional groups directing the peracid to opposite faces of the alkene. The switch to erythro selectivity observed

  将十二个Boc保护的苯丙氨酰基-苯丙氨酸和苯丙氨酰基-甘氨酸反式乙烯基等排物用单过氧邻苯二甲酸镁六水合物（MMPP）和三氟过氧乙酸进行环氧化，并将其结果与早期使用m- CPBA进行环氧化研究的结果进行了比较。使用Julia或Schlosser反应以高收率和高E / Z选择性合成烯烃。在所有环氧化反应中，苏式异构体的形成都受到促进，但在含有两个烯丙基/均烯丙基官能团的基质上将CF 3 CO 3 H导向过酸到烯烃的相对表面上除外。切换到建议使用CF 3 CO 3 H观察到的赤型选择性是通过过酸提供的氢键从配位基向烯丙基酯官能度发出的。其他过酸试剂似乎优先与烯丙基氨基甲酸酯官能团配位。还研究了各个官能团对立体偏好的贡献。
• Stereoselective Epoxidation of Allylic Carbamates with m-Chloroperbenzoic Acid: The Role of Cooperative Coordination
  作者：Annika Jenmalm、Wei Berts、Kristina Luthman、Ingeborg Csoeregh、Uli Hacksell

  DOI：10.1021/jo00109a039

  日期：1995.2

  Stereoselective epoxidations of a series of allylic carbamate methyl esters 1a-d, homoallylic alcohols 1e-h, and acetates 1i-l have been performed using m-chloroperbenzoic acid (m-CPBA) as epoxidizing agent. Throughout, the formation of the three epoxides was favored. This selectivity is probably due to a directing effect of the carbamate group which forms a hydrogen bond to the peracid. However, the threo/erythro isomeric ratio is also dependent on steric interactions and on the possibility of cooperative coordination of the peracid to other suitably positioned functionalities such as allylic methyl ester, homoallylic alcohol, and acetate groups. The results of the present study indicate that the methyl ester is a weaker directing group than the carbamate. However the directing effect of the methyl ester is stronger than that of the homoallylic alcohol and acetate groups. A thermodynamic study of the epoxidation of two epimeric carbamate esters giving considerably different isomeric product ratios (9:1 compared to 2:1) indicates that the order in the transition state structure influences the isomeric ratios.
• Stereoselective Epoxidation of Phe-Gly and Phe-Phe Vinyl Isosteres
  作者：Annika Jenmalm、Wei Berts、Yi-Lin Li、Kristina Luthman、Ingeborg Csoeregh、Uli Hacksell

  DOI：10.1021/jo00084a037

  日期：1994.3

  Novel Phe-Gly and Phe-Phe isosteres have been synthesized. Vinylic isosteres of Phe-Gly and Phe-Phe were prepared by facile Julia reactions, and the resulting stereoisomers were isolated and epoxidized (m-chloroperbenzoic acid). Observed stereoselectivities of epoxidation appear to emanate from a cooperative coordination of the incoming peracid by the carbamate group and the more weakly coordinating allylic ester function.
• Novel synthesis of a Phe-Gly E-alkene dipeptide isostere
  作者：Martin Kranz、Horst Kessler

  DOI：10.1016/0040-4039(96)01108-2

  日期：1996.7

  A new strategy for the synthesis of Boc-Pheψ(E-CHCH)GlyOH (11) is described. The double bond is generated employing a β elimination of the mesyloxy group of 6. This elimination proves to be the key step within the synthesis. Different products are obtained dependent on the base as well as on the reaction conditions. Employing KOtBu leads to E-(5S)-(t-Butyloxycarbonylamino)-6-phenyl-1,3-hexadiene7

  对的Boc-PHE的合成的新策略ψ（Ë -CHCH）GlyOH（11）进行说明。通过β消除6的甲磺酰氧基生成双键。事实证明，这种消除是合成过程中的关键步骤。根据碱以及反应条件获得不同的产物。使用KO t Bu导致E-（5 S）-（叔丁氧羰基氨基）-6-苯基-1,3-己二烯7，而NaOMe导致γ消除，导致氮丙啶9。二烯7转化为相应的Pheψ（E-CH = CH）Gly等排烷烃，随后进行硼氢化和琼斯氧化反应。