[(2R,3S,6S)-3-acetyloxy-6-[2-(4-fluorophenyl)ethynyl]-3,6-dihydro-2H-pyran-2-yl]methyl acetate | 1469874-75-6

• 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: [(2R,3S,6S)-3-acetyloxy-6-[2-(4-fluorophenyl)ethynyl]-3,6-dihydro-2H-pyran-2-yl]methyl acetate
• CAS: 1469874-75-6
• 化学式: C₁₈H₁₇FO₅
• 分子量: 332.328
• InChiKey: XIVJTSKXVMZALL-FGTMMUONSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  24
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  61.8
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  4-氟苯乙炔 、 乙酰化葡萄烯糖 在 C₄₂H₆₃O₃P*C₁₂H₉N₃*CF₃O₃S^(1-)*Au⁽¹⁺⁾ 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 4.0h， 以73%的产率得到[(2R,3S,6S)-3-acetyloxy-6-[2-(4-fluorophenyl)ethynyl]-3,6-dihydro-2H-pyran-2-yl]methyl acetate
  参考文献：
  名称：

  金催化乙烯基醚加氢炔基化：金催化烯烃和炔烃分子间反应的替代途径

  摘要：

  在本报告中，研究了金催化的乙烯基醚和末端炔烃的分子间反应。使用三唑金催化剂减少了乙烯基醚存在下金的分解，并提供了炔基化产物而不是[2 + 2]产物。该方案已扩展到包括糖基底物，该底物经过一锅炔基化-费里尔反应，以中等至优异的产率和高非对映选择性生产功能化糖。

  DOI：

  10.1021/acs.orglett.6b03228

文献信息

• Zinc mediated activation of terminal alkynes: stereoselective synthesis of alkynyl glycosides
  作者：Madhu Babu Tatina、Anil Kumar Kusunuru、Syed Khalid Yousuf、Debaraj Mukherjee

  DOI：10.1039/c4ob01405g

  日期：——

  mediated alkynylation reaction was studied for the preparation of C-glycosides from unactivated alkynes. Different glycosyl donors such as glycals and anomeric acetates were tested towards an alkynyl zinc reagent obtained from alkynes using zinc dust and ethyl bromoacetate as an additive. The method provides simple, mild and stereoselective access to alkynyl glycosides both from aromatic and aliphatic acetylenes

  研究了锌介导的炔基化反应，用于从未活化的炔烃制备C-糖苷。使用锌粉和溴乙酸乙酯作为添加剂，对从炔烃制得的炔基锌试剂进行了测试，测试了不同的糖基供体（例如，乙二醇和异头乙酸酯）。该方法提供了从芳族和脂族乙炔对炔基糖苷的简单，温和和立体选择。
• Transformation of Glycals into α,β,γ,δ-Conjugated Chirons under Metal-Free Conditions
  作者：Tatina Madhubabu、Syed Khalid Yousuf、Anil Kumar Kusunuru、Debaraj Mukherjee

  DOI：10.1002/ejoc.201403041

  日期：2014.11

  A diastereoselective, metal-free, one-pot domino synthetic strategy was developed for the transformation of glycals into new chiral scaffolds. Optimization of the reaction conditions to exclude normal Ferrier products, characterization of the new entities, and a plausible mechanism were investigated.

  开发了一种非对映选择性、无金属、一锅多米诺骨牌合成策略，用于将糖类转化为新的手性支架。研究了排除正常 Ferrier 产物的反应条件优化、新实体的表征和可能的机制。
• Copper mediated stereoselective synthesis of C-glycosides from unactivated alkynes
  作者：Anil Kumar Kusunuru、Madhubabu Tatina、Syed Khalid Yousuf、Debaraj Mukherjee

  DOI：10.1039/c3cc44250k

  日期：——

  A highly stereoselective rapid C-glycosylation reaction has been developed between glycal and unactivated alkynes in the presence of coppertriflate and ascorbic acid at low catalyst loading and at room temperature. A wide variety of glycals and aryl acetylenes participate in the reaction smoothly. TfOH generated during the reduction of Cu(OTf)2 by ascorbic acid may be the active catalyst for the glycosylation.

  在低催化剂载量和室温条件下，在三氟氯酸铜和抗坏血酸存在下，开发出了一种高度立体选择性的甘氨醛和未活化炔烃之间的快速 C-糖基化反应。多种甘氨醛和芳基炔烃顺利地参与了反应。抗坏血酸还原 Cu(OTf)2 时生成的 TfOH 可能是糖基化反应的活性催化剂。
• TMSOTf mediated stereoselective synthesis of α-C-glycosides from unactivated aryl acetylenes
  作者：Heshan Chen、Xiaosheng Luo、Saifeng Qiu、Wengjie Sun、Jianbo Zhang

  DOI：10.1007/s10719-016-9718-7

  日期：2017.2

  A metal free and highly stereoselective procedure for the synthesis of 2,3-unsaturated-C-glycosides has been developed between glycals and unactivated aryl acetylenes in the presence of TMSOTf through a triflated C-vinyl glycosides intermediate. The flexibility of the procedure was tested by a wide variety of glycals and unactivated aryl acetylenes (20 examples). The corresponding alkynyl C-glycosides

  在TMSOTf存在下，通过三氟C-乙烯基糖苷中间体，在糖和未活化的芳基乙炔之间开发了一种无金属且高度立体选择性的合成2,3-不饱和C-糖苷的方法。该方法的灵活性通过多种糖基和未活化的芳基乙炔进行了测试（20个实例）。在短时间内（<25分钟）以高产率获得了具有完全α-选择性的相应炔基C-糖苷。并描述了一个可行的炔基C-糖苷合成机理。