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(S)-(-)-2-Oxo-4,5-dihydro-3H-furan-2-carbonsaeureamid | 91711-84-1

中文名称
——
中文别名
——
英文名称
(S)-(-)-2-Oxo-4,5-dihydro-3H-furan-2-carbonsaeureamid
英文别名
(S)-γ-Butyrolactone-γ-carboxamide;(S)-5-oxotetrahydrofuran-2-carboxamide;(2S)-5-Oxooxolane-2-carboxamide
(S)-(-)-2-Oxo-4,5-dihydro-3H-furan-2-carbonsaeureamid化学式
CAS
91711-84-1
化学式
C5H7NO3
mdl
——
分子量
129.115
InChiKey
AOFIVJOZERJBKG-VKHMYHEASA-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):
    -0.8
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    69.4
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (S)-(-)-2-Oxo-4,5-dihydro-3H-furan-2-carbonsaeureamid 劳森试剂三(2-氯乙基)胺 、 azodicarbonic ethylester 、 叠氮磷酸二苯酯氢气三苯基膦三氟乙酸三氟乙酸酐 作用下, 以 吡啶 为溶剂, 生成 N-t-Butoxycarbonyl-(R)-prolyl-(R)-leucyl-(R)-valyl-2<1-(R)-amino-3-cyano-prop-1-yl>thiazole-4-carboxylic acid ethyl ester
    参考文献:
    名称:
    Schmidt, Ulrich; Utz, Roland, Angewandte Chemie, 1984, vol. 96, # 9, p. 723 - 724
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Construction the A-B Bicyclic Ring Structure of Stemocurtisine
    摘要:
    在这篇论文中,描述了天然产物Stemocurtisine的A-B双环结构3的合成。该合成过程从市售的L-谷氨酸开始,经过七个合成步骤完成。关键步骤涉及hemiaminal 6与反式-β-苯基硼酸和反式-β-苯基氟硼酸钾之间的硼-曼尼希反应,制备顺式二烯4。尝试通过分子内环氧化环开启,然后在不同碱性条件下进行重排来制备A-B-C环化合物2未能成功。唯一未反应的起始物质被回收。
    DOI:
    10.2174/1570178617666200207105649
点击查看最新优质反应信息

文献信息

  • Amino Acids and Peptides; 59.<sup>1</sup>Synthesis of Biologically Active Cyclopeptides; 9.<sup>2</sup>Synthesis of 16 Isomers of Dolastatin 3;<sup>3</sup>I. Synthesis of the 2-(1-aminoalkyl)-thiazole-4-carboxylic Acids
    作者:Ulrich Schmidt、Roland Utz、Albrecht Lieberknecht、Helmut Griesser、Bernd Potzolli、Johanna Bahr、Karin Wagner、Peter Fischer
    DOI:10.1055/s-1987-27899
    日期:——
    The synthesis of the optically active Dolastatin 3 building block 2-(1-amino-3-cyanopropyl)-thiazole-4-carboxylic acid is described as a prerequisite for the total synthesis of dolastatin isomers.
    本文介绍了具有光学活性的多拉他汀 3 结构单元 2-(1-氨基-3-氰丙基)-噻唑-4-羧酸的合成过程,这是全合成多拉他汀异构体的先决条件。
  • Pieper; Trankle; Nieger, Pharmazie, 1995, vol. 50, # 1, p. 15 - 21
    作者:Pieper、Trankle、Nieger、Mohr、Lehmann
    DOI:——
    日期:——
  • Schmidt, Ulrich; Utz, Roland, Angewandte Chemie, 1984, vol. 96, # 9, p. 723 - 724
    作者:Schmidt, Ulrich、Utz, Roland
    DOI:——
    日期:——
  • Construction the A-B Bicyclic Ring Structure of Stemocurtisine
    作者:Duc Dau Xuan
    DOI:10.2174/1570178617666200207105649
    日期:2021.1
    <p>In this paper, the synthesis of the A-B bicyclic ring structure 3 of the natural product Stemocurtisine is described. The synthesis was accomplished in seven synthetic steps from commercially available L-glutamic acid. The key step involved a borono-Mannich reaction between the hemiaminal 6 and trans-&#946;-styryl boronic acid and trans-&#946;-styrylpotassiumtrifluoroborate to prepare the cis diene 4. Attempts to prepare the A-B-C ring compound 2 via intramolecular epoxide ring opening followed by rearrangement under different basic conditions were unsuccessful. The only unreactive starting material was recovered.</p> </sec></div> <div class="value-text ch">在这篇论文中,描述了天然产物Stemocurtisine的A-B双环结构3的合成。该合成过程从市售的L-谷氨酸开始,经过七个合成步骤完成。关键步骤涉及hemiaminal 6与反式-β-苯基硼酸和反式-β-苯基氟硼酸钾之间的硼-曼尼希反应,制备顺式二烯4。尝试通过分子内环氧化环开启,然后在不同碱性条件下进行重排来制备A-B-C环化合物2未能成功。唯一未反应的起始物质被回收。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101bf8y0c6447f150N0&inchikey=AOFIVJOZERJBKG-VKHMYHEASA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_216" class="compound-item" title="(+)-(3R)-3-{[叔丁基(二甲基)硅基]氧基}二氢呋喃-2(3H)-酮">(+)-(3R)-3-{[叔丁基(二甲基)硅基]氧基}二氢呋喃-2(3H)-酮</a> <a target="_blank" href="https://www.molaid.com/MS_227" class="compound-item" title="龙胆黄碱">龙胆黄碱</a> <a target="_blank" href="https://www.molaid.com/MS_231" 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