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Boc-L-Phe-Z-ΔAbu(β-Br)-OMe | 1107651-62-6

中文名称
——
中文别名
——
英文名称
Boc-L-Phe-Z-ΔAbu(β-Br)-OMe
英文别名
methyl (Z)-3-bromo-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]but-2-enoate
Boc-L-Phe-Z-ΔAbu(β-Br)-OMe化学式
CAS
1107651-62-6
化学式
C19H25BrN2O5
mdl
——
分子量
441.322
InChiKey
PHXGYTDSYMZQKE-UZFBZYOGSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    27
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    93.7
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    Boc-L-Phe-Z-ΔAbu(β-Br)-OMe1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 乙腈 为溶剂, 反应 0.5h, 以78%的产率得到(S)-methyl 2-(1-((tert-butoxycarbonyl)amino)-2-phenylethyl)-5-methyloxazole-4-carboxylate
    参考文献:
    名称:
    A mild high yielding synthesis of oxazole-4-carboxylate derivatives
    摘要:
    Several 2,5-disubstituted oxazole-4-carboxylates were prepared in high yields from the methyl esters of N-acyl-beta-halodehydroaminobutyric acid derivatives by treatment with a 2% solution of DBU in acetonitrile. The scope of this reaction was investigated and it was found that dehydrodipeptides having a beta-bromodehydroaminobutyric acid residue gave the corresponding oxazoles in good yields. The photophysical properties of some of the oxazoles prepared were studied in four solvents of different polarity. All compounds have reasonable high fluorescence quantum yields and a moderate solvent sensitivity, which makes them good candidates to be used as fluorescent probes. One of the fluorescent oxazoles prepared was inserted after cleavage of the methyl ester into two model peptides using a conventional solution phase strategy. The photophysical properties of the labelled peptides were studied in ethanol and water and compared with those of the oxazole. The results obtained showed that the oxazole maintains a good fluorescence level and the same solvent sensitivity when linked to a peptide chain. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.09.014
  • 作为产物:
    描述:
    Boc-L-Phe-Z-ΔAbu-OMe 在 N-溴代丁二酰亚胺(NBS) 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 生成 Boc-L-Phe-Z-ΔAbu(β-Br)-OMeBoc-L-Phe-E-ΔAbu(β-Br)-OMe
    参考文献:
    名称:
    芘氨基酸:合成、光物理和电化学研究
    摘要:
    几种β-芘基脱氢氨基酸和芘基丙氨酸衍生物已通过几种类型的反应从脱氢氨基酸以良好到高的产率合成。β-[(芘-1-基)甲基氨基]丙氨酸是通过在过量存在下用(芘-1-基)甲胺盐酸盐处理N,N-(二-叔丁氧基羰基)脱氢丙氨酸甲酯制备的。碳酸钾。N-(叔丁氧基羰基)-β-(1,2,4-三唑-1-基)脱氢丙氨酸和脱氢氨基丁酸甲酯的E异构体在存在下用(芘-1-基)甲胺盐酸盐处理三乙胺生成β-氨基甲基芘脱氢丙氨酸和脱氢氨基丁酸衍生物的E异构体。β-(芘-1-基)脱氢苯丙氨酸和脱氢氨基丁酸衍生物通过铃木交叉偶联从相应的β-溴脱氢氨基酸和(芘-1-基)硼酸的纯立体异构体中获得。该反应也成功地应用于β-溴脱氢二肽。通过循环伏安法研究了一些制备的化合物的电化学行为。芘丙氨酸氧化和还原的峰值电位与芘报道的峰值电位相似。然而,发现当芘环与脱氢氨基酸部分共轭时,这些化合物比芘具有更高的氧化和还原峰电位。在环己烷和醇中评
    DOI:
    10.1002/ejoc.200800640
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文献信息

  • Synthesis and electrochemical behaviour of β-halodehydroamino acid derivatives
    作者:Paula M. T. Ferreira、L. S. Monteiro、G. Pereira
    DOI:10.1007/s00726-009-0466-x
    日期:2010.7
    conclude that when N-iodosuccinimide was used as reagent a much higher Z-stereoselectivity is found. The electrochemical behaviour of the halogenated dehydroamino acids was studied by cyclic voltammetry. The results show a shift in the reduction peak to higher potentials of the β-halogenated dehydroamino acids when compared with the corresponding non-halogenated derivatives. As expected, the β,β-dihalodehydroalanines
    通过使相应的脱氢氨基酸衍生物与N-卤代琥珀酰亚胺或在β,β-二碘代十二氢丙氨酸与碘反应的情况下,合成了几种新的β,β-二卤代和β-卤代-β-取代的脱氢丙氨酸和脱氢二肽。获得的结果证实,与β-取代的脱氢氨基酸的卤化反应的立体化学结果取决于底物。因此,当将β-苯基脱氢丙氨酸用作底物并且当这些化合物被4-甲苯磺酰基或氨基甲酸酯N-保护时,发现Z-立体选择性增加。从这项研究中,也有可能得出结论,当N-碘代琥珀酰亚胺用作试剂,发现更高的Z-立体选择性。通过循环伏安法研究了卤代脱氢氨基酸的电化学行为。结果表明,与相应的非卤代衍生物相比,β-卤代脱氢氨基酸的还原峰向更高的电位转移。如所预期的,与相应的碘代脱氢氨基酸相比,β,β-二卤代氢丙氨酸显示出比β-卤代-β-取代的脱氢丙氨酸更高的峰势,并且溴衍生物具有更低的峰势。几种β-卤代-β-取代的脱氢氨基酸的受控电势电解以其E和Z异构体的混合物形式提供了相应
  • Pyrenylamino Acids: Synthesis, Photophysical and Electrochemical Studies
    作者:Ana S. Abreu、Elisabete M. S. Castanheira、Paula M. T. Ferreira、Luís S. Monteiro、Goreti Pereira、Maria-João R. P. Queiroz
    DOI:10.1002/ejoc.200800640
    日期:2008.12
    This reaction was also applied successfully to β-bromodehydrodipeptides. The electrochemical behaviour of some of the compounds prepared was studied by cyclic voltammetry. The peak potentials for the oxidation and reduction of pyrenylalanines were similar to those reported for pyrene. However, it was found that when the pyrene ring was conjugated with the dehydroamino acid moiety, the compounds had
    几种β-芘基脱氢氨基酸和芘基丙氨酸衍生物已通过几种类型的反应从脱氢氨基酸以良好到高的产率合成。β-[(芘-1-基)甲基氨基]丙氨酸是通过在过量存在下用(芘-1-基)甲胺盐酸盐处理N,N-(二-叔丁氧基羰基)脱氢丙氨酸甲酯制备的。碳酸钾。N-(叔丁氧基羰基)-β-(1,2,4-三唑-1-基)脱氢丙氨酸和脱氢氨基丁酸甲酯的E异构体在存在下用(芘-1-基)甲胺盐酸盐处理三乙胺生成β-氨基甲基芘脱氢丙氨酸和脱氢氨基丁酸衍生物的E异构体。β-(芘-1-基)脱氢苯丙氨酸和脱氢氨基丁酸衍生物通过铃木交叉偶联从相应的β-溴脱氢氨基酸和(芘-1-基)硼酸的纯立体异构体中获得。该反应也成功地应用于β-溴脱氢二肽。通过循环伏安法研究了一些制备的化合物的电化学行为。芘丙氨酸氧化和还原的峰值电位与芘报道的峰值电位相似。然而,发现当芘环与脱氢氨基酸部分共轭时,这些化合物比芘具有更高的氧化和还原峰电位。在环己烷和醇中评
  • A mild high yielding synthesis of oxazole-4-carboxylate derivatives
    作者:Paula M.T. Ferreira、Elisabete M.S. Castanheira、Luís S. Monteiro、Goreti Pereira、Helena Vilaça
    DOI:10.1016/j.tet.2010.09.014
    日期:2010.11
    Several 2,5-disubstituted oxazole-4-carboxylates were prepared in high yields from the methyl esters of N-acyl-beta-halodehydroaminobutyric acid derivatives by treatment with a 2% solution of DBU in acetonitrile. The scope of this reaction was investigated and it was found that dehydrodipeptides having a beta-bromodehydroaminobutyric acid residue gave the corresponding oxazoles in good yields. The photophysical properties of some of the oxazoles prepared were studied in four solvents of different polarity. All compounds have reasonable high fluorescence quantum yields and a moderate solvent sensitivity, which makes them good candidates to be used as fluorescent probes. One of the fluorescent oxazoles prepared was inserted after cleavage of the methyl ester into two model peptides using a conventional solution phase strategy. The photophysical properties of the labelled peptides were studied in ethanol and water and compared with those of the oxazole. The results obtained showed that the oxazole maintains a good fluorescence level and the same solvent sensitivity when linked to a peptide chain. (C) 2010 Elsevier Ltd. All rights reserved.
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