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5-deoxy-D-arabino-heptulose

中文名称
——
中文别名
——
英文名称
5-deoxy-D-arabino-heptulose
英文别名
(2S,3S,4R,6S)-2,6-bis(hydroxymethyl)oxane-2,3,4-triol
5-deoxy-D-arabino-heptulose化学式
CAS
——
化学式
C7H14O6
mdl
——
分子量
194.185
InChiKey
SZLDLWDSWBSNAP-VZFHVOOUSA-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):
    -2.5
  • 重原子数:
    13
  • 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:
    110
  • 氢给体数:
    5
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    5-deoxy-D-arabino-heptulose 在 Dowex 50(H+) 作用下, 以 甲醇 为溶剂, 生成 2,7-anhydro-5-deoxy-D-arabino-heptulose
    参考文献:
    名称:
    Sequential One-Pot Aldol Reactions Catalyzed by 2-Deoxyribose-5-phosphate Aldolase and Fructose-1,6-diphosphate Aldolase
    摘要:
    DOI:
    10.1021/ja00115a038
  • 作为产物:
    参考文献:
    名称:
    Sequential One-Pot Aldol Reactions Catalyzed by 2-Deoxyribose-5-phosphate Aldolase and Fructose-1,6-diphosphate Aldolase
    摘要:
    DOI:
    10.1021/ja00115a038
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文献信息

  • Sequential Three- and Four-Substrate Aldol Reactions Catalyzed by Aldolases
    作者:Harrie J. M. Gijsen、Chi-Huey Wong
    DOI:10.1021/ja00134a001
    日期:1995.7
    This paper describes a useful synthetic strategy based on sequential enzyme-catalyzed aldol addition reactions. The aldol reaction of an acceptor aldehyde with acetaldehyde, catalyzed by 2-deoxyribose-5-phosphate aldolase (DERA, EC 4.1.2.4), gives a new aldehyde, which subsequently reacts with a second donor substrate, catalyzed by DERA or another aldolase. This sequential aldol reaction proceeds because of the formation of a stable cyclic hemiacetal or hemiketal product. In this way several 6-substituted 2,4,6-trideoxyhexoses have been stereoselectively synthesized via a one-pot double DERA-catalyzed reaction. DERA coupled with fructose-1,6-diphosphate aldolase from rabbit muscle (RAMA, EC 4.1.2.13) in a one-pot reaction gave a variety of 5-deoxyheptuloses, however not in 100% stereoselectivity. The sequential aldol reactions with four substrates were accomplished by coupling DERA with N-acetylneuraminic acid aldolase (NeuAc aldolase, EC 4.1.3.3) to give several nine-carbon sialic acid-type sugar derivatives.
  • Sequential One-Pot Aldol Reactions Catalyzed by 2-Deoxyribose-5-phosphate Aldolase and Fructose-1,6-diphosphate Aldolase
    作者:Harrie J. M. Gijsen、Chi-Huey Wong
    DOI:10.1021/ja00115a038
    日期:1995.3
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