methyl 5-deoxy-5-iodo-D-arabinofuranoside | 281678-19-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: methyl 5-deoxy-5-iodo-D-arabinofuranoside
• 英文别名: methyl 5-deoxy-5-iodo-D-arabinoside；5-iodo-1-O-methyl-D-arabinofuranoside；(2S,3S,4S)-2-(iodomethyl)-5-methoxyoxolane-3,4-diol
• CAS: 281678-19-1
• 化学式: C₆H₁₁IO₄
• 分子量: 274.055
• InChiKey: WYMYPTFVMQUWRR-VRPWFDPXSA-N

物化性质

• 沸点：
  367.3±42.0 °C(Predicted)
• 密度：
  1.96±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  58.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl 5-deoxy-5-iodo-D-arabinofuranoside 在 ammonium acetate 、 氨 、 sodium cyanoborohydride 、 锌 、 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 18.0h， 以93%的产率得到(2R,3R)-1-aminopent-4-ene-2,3-diol hydrochloride
  参考文献：
  名称：

  胺的无保护基团合成：通过还原胺化由醛类合成伯胺

  摘要：

  提出了一种新的无保护基合成伯胺的方法。通过优化金属氢化物/氨介导的醛和半缩醛的还原胺化反应，可以选择性地制备伯胺，而不会或很少会形成通常的仲胺和叔胺副产物。该方法是在一系列功能化的醛底物上进行的，包括从Vasella反应中原位形成的醛。这些还原性胺化条件提供了有价值的合成工具，用于以较少的步骤，良好的收率并且不使用保护基团来选择性生产伯胺。

  DOI：

  10.1021/jo100004c
• 作为产物：
  描述：

  甲基 D-阿糖胞苷 在 吡啶 、 sodium iodide 作用下， 以 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 生成 methyl 5-deoxy-5-iodo-D-arabinofuranoside
  参考文献：
  名称：

  5-硫代己吡喃糖苷的新型合成：5-硫代-d-和l-葡萄糖和1,6-脱水5-硫代-1-和d-altrose的制备

  摘要：

  描述了5-硫代葡萄糖和1，6-脱水-5-硫代altrose的d-和l-异构体的不对称合成。关键中间体1-苏糖和d-苏糖二乙缩醛衍生物是通过化学转化衍生自d-木糖或d-阿拉伯糖，以及通过Sharpless不对称二羟基化而得自γ-羟基丙烯醛二乙基缩醛。他们在七个步骤中通过反式-2,3-环氧醇转化为γ-噻吩基二乙缩醛。乙酸促进的γ-噻喃基二乙基缩醛的环化反应生成5-硫代吡喃糖苷。在酸性条件下除去保护基，分别得到5-硫代-d-和1-葡萄糖和1，6-脱水-5-硫代-1-和d-altrose。

  DOI：

  10.1016/s0040-4020(03)00864-0

文献信息

• Glycomimetic Building Blocks: A Divergent Synthesis of Epimers of Shikimic Acid
  作者：Joseph C. Grim、Kathleen C. A. Garber、Laura L. Kiessling

  DOI：10.1021/ol201252x

  日期：2011.8.5

  A divergent synthesis of (−)-4-epi-shikimic acid was developed. This route features a one-pot zinc-mediated reductive ring opening of an arabinofuranose followed by a Barbier reaction and culminates in a ring-closing metathesis. Functionalization of (−)-4-epi-shikimic acid via conjugate addition of a thiol occurs in high diastereoselectivity to afford a product with the features of fucosylated glycans

  开发了(-)-4-表-莽草酸的发散合成。该路线的特点是一锅锌介导的阿拉伯呋喃糖还原开环，然后是巴比耶反应，最后是闭环复分解。(-)-4-表-莽草酸通过硫醇的共轭加成以高非对映选择性进行官能化，以提供具有岩藻糖基化聚糖特征的产物。
• [EN] METHODS FOR THE PREPARATION OF ALKENYLAMINES, CYCLIC CARBAMATES OR DITHIOCARBAMATES, AND AMINOALCOHOLS OR AMINOTHIOLS<br/>[FR] PROCÉDÉS POUR LA PRÉPARATION D'ALCÉNYLAMINES, DE CARBAMATES CYCLIQUES OU DE DITHIOCARBAMATES, ET D'AMINOALCOOLS OU D'AMINOTHIOLS
  申请人：VICTORIA LINK LTD

  公开号：WO2010041964A1

  公开（公告）日：2010-04-15

  A method for preparing an alkenylamine, or a salt, solvate or hydrate thereof, is disclosed. The method comprises reacting a alogen-substituted cyclic acetal or a derivative thereof under particular conditions to provide the alkenylamine, which may be optionally converted into a salt, solvate or hydrate thereof. A method for preparing a cyclic carbamate or cyclic dithiocarbamate, or a salt, solvate or hydrate thereof, is also disclosed. The method comprises reacting an alkenylamine under particular conditions to provide the cyclic carbamate or cyclic dithiocarbamate, which may be optionally converted into a salt, solvate or hydrate thereof. A method for preparing a 1,2-aminoalcohol or 1,2-aminothiol, or a salt, solvate or hydrate thereof, is also disclosed. The method comprises forming a cyclic carbamate or cyclic dithiocarbamate from an alkenylamine, and deprotecting the cyclic carbamate or cyclic dithiocarbamate to provide the 1,2-aminoalcohol or 1,2-aminothiol, which may optionally be converted into a salt, solvate or hydrate thereof.

  揭示了一种制备烯基胺或其盐、溶剂合物或水合物的方法。该方法包括在特定条件下反应氯代取代的环缩醛或其衍生物以提供烯基胺，该烯基胺可以选择性地转化为其盐、溶剂合物或水合物。还揭示了一种制备环氨基甲酸酯或环二硫代氨基甲酸酯或其盐、溶剂合物或水合物的方法。该方法包括在特定条件下反应烯基胺以提供环氨基甲酸酯或环二硫代氨基甲酸酯，该化合物可以选择性地转化为其盐、溶剂合物或水合物。还揭示了一种制备1,2-氨基醇或1,2-氨基硫醇或其盐、溶剂合物或水合物的方法。该方法包括从烯基胺中形成环氨基甲酸酯或环二硫代氨基甲酸酯，并去保护环氨基甲酸酯或环二硫代氨基甲酸酯以提供1,2-氨基醇或1,2-氨基硫醇，该化合物可以选择性地转化为其盐、溶剂合物或水合物。
• Synthesis and anti-tuberculosis activity of glycitylamines
  作者：Hilary M. Corkran、Emma M. Dangerfield、Gregory W. Haslett、Bridget L. Stocker、Mattie S.M. Timmer

  DOI：10.1016/j.bmc.2015.12.036

  日期：2016.2

  A series of glycitylamines, which were prepared in few steps from readily available carbohydrates, were tested for their ability to inhibit tuberculosis growth in an Alamar Blue BCG colourimetric assay. Several derivatives, including (2R, 3R)-1-(hexadecylamine)pent-4-ene-2,3-diol, (2R, 3R)-1-(hexadecylmethylamino)pent-4-ene-2,3-diol and 5-deoxy-5-hexadecylmethylamino-D-arabinitol, were prepared in good to excellent (44-90%) overall yield and exhibited micromolar (20-41 mu M) inhibitory activity that was similar to the first line tuberculosis (TB) drug ethambutol (39 mu M) in the same assay. The ease and low cost of the synthesis of the glycitylamines offers definite advantages for their use as potential TB drugs. (c) 2016 Elsevier Ltd. All rights reserved.
• Synthesis of difluorinated carbocyclic analogues of 5-deoxypentofuranoses and 1-amino-5-deoxypentofuranoses: en route to fluorinated carbanucleosides
  作者：Gaëlle Fourrière、Nathalie Van Hijfte、Jérôme Lalot、Guy Dutech、Bruno Fragnet、Gaël Coadou、Jean-Charles Quirion、Eric Leclerc

  DOI：10.1016/j.tet.2010.03.079

  日期：2010.5

  The synthesis of difluorinated carbocyclic analogues of 5-deoxypentofuranoses and 1-amino-5-deoxypentofuranoses is described. The sequence involves an addition of PhSeCF2TMS to carbohydrate-derived aldehydes or their corresponding tert-butanesulfinylimines followed by a radical cyclization. Optimized conditions for the PhSeCF2TMS addition to alpha-chiral aldehydes have been disclosed and its unusual diastereoselectivity is discussed. Application of the sequence using Ellman's auxiliary allows a more direct access to 1-aminopentose analogues with a complete control of the pseudo-anomeric center configuration. (C) 2010 Elsevier Ltd. All rights reserved.
• A fast, efficient and stereoselective synthesis of hydroxy-pyrrolidines
  作者：Emma M. Dangerfield、Shivali A. Gulab、Catherine H. Plunkett、Mattie S.M. Timmer、Bridget L. Stocker

  DOI：10.1016/j.carres.2010.03.016

  日期：2010.7

  A five-step, protecting group free synthesis of 2,3-cis substituted hydroxy-pyrrolidines is presented. Key steps in the synthesis are the chemoselective formation of a primary amine via a Vasella reductive amination using ammonia as the nitrogen source, and the stereoselective formation of a cyclic carbamate from an alkenylamine. Improvement of the reductive amination, by way of the use of alpha-picoline borane as a more environmentally benign reducing agent, is also presented. (C) 2010 Elsevier Ltd. All rights reserved.