(S)-1-Azido-2-octanol | 124817-03-4

• 分子结构分类: 有机化合物 - 有机1,3-偶极化合物 - 烯丙基型1,3-偶极有机化合物
• 英文名称: (S)-1-Azido-2-octanol
• 英文别名: (R,S)-1-Azido-octan-2-ol；(2S)-1-azidooctan-2-ol
• CAS: 124817-03-4
• 化学式: C₈H₁₇N₃O
• 分子量: 171.242
• InChiKey: NBYVTGUZUJZLHG-QMMMGPOBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  12
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  34.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  (S)-(-)-1,2-辛二醇 在 叠氮基三甲基硅烷 、 偶氮二甲酸二异丙酯 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 生成 (S)-1-Azido-2-octanol
  参考文献：
  名称：

  Regioselective and Stereospecific Azidation of 1,2- and 1,3-Diols by Azidotrimethylsilane via a Mitsunobu Reaction

  摘要：

  A one-pot regio- and stereospecific azidation reaction of 1,2- and 1,3-diols with azidotrimethylsilane (Me3SiN3) via a Mitsunobu reaction has been achieved. With 1,2- and 1,3-diols, the reaction of triphenylphosphine, diisopropyl azodicarboxylate, and Me3SiN3 in dichloromethane gave regioselective azidation at C-2 and C-3, respectively, in good yield (74-90% combined yield of 1a + 1b or of 2a + 2b). However, application of the same reaction conditions to a 1,4-diol led to the exclusive formation of the cyclic ether. The regioselectivity of this one-pot reaction is influenced by the solvent, the degree of steric bulk at C-2 of the 1,2-diol or at C-3 of the 1,3-diol, and the presence of electron-donating and electron-withdrawing groups near the secondary carbinol carbon. This selectivity is discussed in terms of the mechanistic model proposed by Mathieu-Pelta and Evans (Mathieu-Pelta, I.; Evans, S. A., Jr. J. Org. Chem. 1898, 57, 3409-3413), which involves reaction of the dioxaphospholane intermediate with Me3SiN3 to form oxyphosphonium ions 4 and 5.

  DOI：

  10.1021/jo9906375

文献信息

• Biocatalytic Cascade for the Synthesis of Enantiopure β-Azidoalcohols and β-Hydroxynitriles
  作者：Joerg H. Schrittwieser、Iván Lavandera、Birgit Seisser、Barbara Mautner、Wolfgang Kroutil

  DOI：10.1002/ejoc.200900091

  日期：2009.5

  one-pot reaction sequence starting from prochiral α-chloroketones leading to enantiopure β-azidoalcohols and β-hydroxynitriles is described. Asymmetric bioreduction of α-chloroketones by hydrogen transfer catalysed by an alcohol dehydrogenase (ADH) established the stereogenic centre in the first step to furnish enantiopure chlorohydrin intermediates. Subsequent biocatalysed ring closure to the epoxide

  描述了从前手性 α-氯酮开始导致对映纯 β-叠氮醇和 β-羟基腈的三步、两酶、一锅反应序列。通过由醇脱氢酶 (ADH) 催化的氢转移对 α-氯酮进行不对称生物还原，在第一步中建立了立体中心，以提供对映纯的氯醇中间体。随后通过非选择性卤代醇脱卤酶 (Hhe) 催化环氧化物的生物催化闭环和用叠氮化物 N3- 或氰化物 CN- 的亲核开环进行完全保留构型，得到对映体纯的 β-叠氮醇和 β-羟基腈，分别。合成了各种光学纯 β-叠氮醇和 β-羟基腈的两种对映异构体。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
• Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols
  作者：Aníbal Cuetos、Fabricio R. Bisogno、Iván Lavandera、Vicente Gotor

  DOI：10.1039/c3cc38674k

  日期：——

  The combination of biocatalysis and ‘click’ chemistry is shown to obtain chiral 1,2,3-triazole diols in a fully convergent one-pot two-step synthesis.

  生物催化和“点击”化学的结合被证明可以在完全汇聚的一锅两步合成中获得手性1,2,3-三唑二醇。
• Lipase-catalyzed resolution of acyclic amino alcohol precursors
  作者：Eva Foelsche、Andrea Hickel、Helmut Hoenig、Peter Seufer-Wasserthal

  DOI：10.1021/jo00293a015

  日期：1990.3
• FOELSCHE, EVA;HICKEL, ANDREA;HONIG, HELMUT;SEUFER-WASSERTHAL, PETER, J. ORG. CHEM., 55,(1990) N, C. 1749-1753
  作者：FOELSCHE, EVA、HICKEL, ANDREA、HONIG, HELMUT、SEUFER-WASSERTHAL, PETER

  DOI：——

  日期：——