1-deoxy-L-allitol | 95120-27-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-deoxy-L-allitol
• 英文别名: L-1-deoxy-allitol；D-allomethylitol；D-Allomethylit；6-Deoxy-β-D-allofuranosid；6-Deoxyallitol；(2S,3S,4R,5R)-hexane-1,2,3,4,5-pentol
• CAS: 95120-27-7
• 化学式: C₆H₁₄O₅
• 分子量: 166.174
• InChiKey: SKCKOFZKJLZSFA-MOJAZDJTSA-N

物化性质

• 熔点：
  116-119 °C
• 沸点：
  468.0±40.0 °C(Predicted)
• 密度：
  1.424±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -2
• 重原子数：
  11
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  101
• 氢给体数：
  5
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  1-deoxy-L-allitol 在 Enterobacter aerogenes IK₇ 作用下， 以 水 为溶剂， 以100%的产率得到6-Desoxy-D-psicose
  参考文献：
  名称：

  Conversion of l-rhamnose into ten of the sixteen 1- and 6-deoxyketohexoses in water with three reagents: d-tagatose-3-epimerase equilibrates C3 epimers of deoxyketoses

  摘要：

  The efficient isomerization of L-rhamnose [the only cheaply available deoxy hexose] to 1-deoxy-L-psicose, 1-deoxy-D-psicose, 1-deoxy-L-fructose, 1-deoxy-D-fructose, 1-deoxy-L-tagatose, 6-deoxy-L-psicose, 6-deoxy-D-psicose, 6-deoxy-L-fructose, 6-deoxy-D-fructose, and 6-deoxy-L-tagatose is described. The conversion of rhamnose to ten of the sixteen 1- and 6-deoxyketohexoses is accomplished in water in three steps. The range of substrates for D-tagatose-3-epimerase (DTE) is extended to 1- and 6-deoxyketoses. An authentic sample of 6-deoxy-D-psicose is prepared from D-psicose. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.12.024
• 作为产物：
  描述：

  methyl 6-deoxy-β-D-allofuranoside 生成 1-deoxy-L-allitol
  参考文献：
  名称：

  Buchanan; Edgar; Power, Journal of the Chemical Society. Perkin transactions I, 1974, vol. 0, # 16, p. 1943 - 1949

  摘要：

  DOI：

文献信息

• DEOXYKETOHEXOSE ISOMERASE AND METHOD FOR PRODUCING DEOXYHEXOSE AND DERIVATIVE THEREOF USING SAME
  申请人：Izumori Ken

  公开号：US20100105885A1

  公开（公告）日：2010-04-29

  Providing 1- or 6-deoxy products corresponding to all of aldohexoses, ketohexoses and sugar alcohols, as based on Deoxy-Izumoring, as well as a method for systematically producing those products. A method for producing deoxyketohexose and a derivative thereof using a deoxyketohexose isomerase derived from Pseudomonas cichorii ST-24 (FERM BP-2736), comprising epimerizing 1-deoxy D-ketohexose or 6-deoxy D-ketohexose or 1-deoxy L-ketohexose or 6-deoxy L-ketohexose at position 3 to produce the individually corresponding 1-deoxy D-ketohexose or 6-deoxy D-ketohexose or 1-deoxy L-ketohexose or 6-deoxy L-ketohexose as an intended product.

  提供与所有醛糖、酮糖和糖醇对应的1-或6-去氧产物，基于Deoxy-Izumoring，以及系统生产这些产品的方法。使用源自Pseudomonas cichorii ST-24（FERM BP-2736）的去氧酮糖异构酶，包括在位置3上使1-去氧D-酮糖、6-去氧D-酮糖、1-去氧L-酮糖或6-去氧L-酮糖的环式异构化，以产生相应的1-去氧D-酮糖、6-去氧D-酮糖、1-去氧L-酮糖或6-去氧L-酮糖作为预期产物的方法。
• Deoxyketohexose isomerase and method for producing deoxyhexose and derivative thereof using same
  申请人：Izumori Ken

  公开号：US08389248B2

  公开（公告）日：2013-03-05

  Providing 1- or 6-deoxy products corresponding to all of aldohexoses, ketohexoses and sugar alcohols, as based on Deoxy-Izumoring, as well as a method for systematically producing those products. A method for producing deoxyketohexose and a derivative thereof using a deoxyketohexose isomerase derived from Pseudomonas cichorii ST-24 (FERM BP-2736), comprising epimerizing 1-deoxy D-ketohexose or 6-deoxy D-ketohexose or 1-deoxy L-ketohexose or 6-deoxy L-ketohexose at position 3 to produce the individually corresponding 1-deoxy D-ketohexose or 6-deoxy D-ketohexose or 1-deoxy L-ketohexose or 6-deoxy L-ketohexose as an intended product.

  提供所有醛糖、酮糖和糖醇对应的1-或6-去氧产物，基于Deoxy-Izumoring，以及一种系统生产这些产物的方法。使用源自Pseudomonas cichorii ST-24 (FERM BP-2736)的去氧酮糖异构酶，包括在位置3上使1-去氧D-酮糖、6-去氧D-酮糖、1-去氧L-酮糖或6-去氧L-酮糖发生外消旋反应，以生产相应的1-去氧D-酮糖、6-去氧D-酮糖、1-去氧L-酮糖或6-去氧L-酮糖作为预期产物的方法。
• Characterization of 6-deoxy-d-altritol in the cell-wall polysaccharide of Nocardia asteroides R 399
  作者：Annie Voiland、Georges Michel

  DOI：10.1016/s0008-6215(00)90459-2

  日期：1985.9

  A polyol, found in the cell-wall of Nocardia asteroides R 399 as a component of a neutral polysaccharide mainly composed of D-arabinose and D-galactose, was identified by mass spectrometry, paper chromatography, thin-layer chromatography, and gas chromatography as 6-deoxy-D-altritol.
• Iwadare, Bulletin of the Chemical Society of Japan, 1942, vol. 17, p. 301
  作者：Iwadare

  DOI：——

  日期：——
• Conversion of l-rhamnose into ten of the sixteen 1- and 6-deoxyketohexoses in water with three reagents: d-tagatose-3-epimerase equilibrates C3 epimers of deoxyketoses
  作者：Pushpakiran Gullapalli、Akihide Yoshihara、Kenji Morimoto、Devendar Rao、Kazuya Akimitsu、Sarah F. Jenkinson、George W.J. Fleet、Ken Izumori

  DOI：10.1016/j.tetlet.2009.12.024

  日期：2010.2

  The efficient isomerization of L-rhamnose [the only cheaply available deoxy hexose] to 1-deoxy-L-psicose, 1-deoxy-D-psicose, 1-deoxy-L-fructose, 1-deoxy-D-fructose, 1-deoxy-L-tagatose, 6-deoxy-L-psicose, 6-deoxy-D-psicose, 6-deoxy-L-fructose, 6-deoxy-D-fructose, and 6-deoxy-L-tagatose is described. The conversion of rhamnose to ten of the sixteen 1- and 6-deoxyketohexoses is accomplished in water in three steps. The range of substrates for D-tagatose-3-epimerase (DTE) is extended to 1- and 6-deoxyketoses. An authentic sample of 6-deoxy-D-psicose is prepared from D-psicose. (C) 2009 Elsevier Ltd. All rights reserved.