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6,1',6'-tri-O-acetyl-2,3':3,4-dianhydro-4'-O-tosyl-allo-sucrose | 131158-15-1

中文名称
——
中文别名
——
英文名称
6,1',6'-tri-O-acetyl-2,3':3,4-dianhydro-4'-O-tosyl-allo-sucrose
英文别名
[(1R,3S,5R,6R,7S,9R,10R,12R,13R)-3,5-bis(acetyloxymethyl)-6-(4-methylphenyl)sulfonyloxy-2,4,8,11,14-pentaoxatetracyclo[7.5.0.03,7.010,12]tetradecan-13-yl]methyl acetate
6,1',6'-tri-O-acetyl-2,3':3,4-dianhydro-4'-O-tosyl-allo-sucrose化学式
CAS
131158-15-1
化学式
C25H30O14S
mdl
——
分子量
586.571
InChiKey
VNZGDQAKZIAGHN-OVISOGSZSA-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):
    0.2
  • 重原子数:
    40
  • 可旋转键数:
    12
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    180
  • 氢给体数:
    0
  • 氢受体数:
    14

反应信息

  • 作为反应物:
    描述:
    三苯基氯甲烷6,1',6'-tri-O-acetyl-2,3':3,4-dianhydro-4'-O-tosyl-allo-sucrose吡啶sodium methylate 作用下, 生成 2,3':3,4-dianhydro-4'-O-tosyl-6,1',6'-tri-O-trityl-allo-sucrose
    参考文献:
    名称:
    2,3′-anhydrosucrose
    摘要:
    Alkaline hydrolysis of alpha-D-glucopyranosyl 3,4-anhydro-beta-D-ribo-hexulofuranoside (1) involves participation of HO-2 and leads to 2,3'-anhydrosucrose (2). The structure of 2 was assigned on the basis of the n.m.r. and mass spectra of its hexa-acetate 3 and confirmed by the formation from 2 of the 6,6'-di-(4) and 6,1',6'-tri-O-trityl (5) derivatives, the 4,6-O-isopropylidene derivative (6), and 2,3':3,4-dianhydro-galacto-sucrose, isolated as the tetra-acetate 7. The structure of 7 was confirmed by its conversion into the 4'-O-tosyl-6,1',6'-O-trityl derivative 14 and by unambiguous synthesis from 6.
    DOI:
    10.1016/0008-6215(90)80136-q
  • 作为产物:
    参考文献:
    名称:
    2,3′-anhydrosucrose
    摘要:
    Alkaline hydrolysis of alpha-D-glucopyranosyl 3,4-anhydro-beta-D-ribo-hexulofuranoside (1) involves participation of HO-2 and leads to 2,3'-anhydrosucrose (2). The structure of 2 was assigned on the basis of the n.m.r. and mass spectra of its hexa-acetate 3 and confirmed by the formation from 2 of the 6,6'-di-(4) and 6,1',6'-tri-O-trityl (5) derivatives, the 4,6-O-isopropylidene derivative (6), and 2,3':3,4-dianhydro-galacto-sucrose, isolated as the tetra-acetate 7. The structure of 7 was confirmed by its conversion into the 4'-O-tosyl-6,1',6'-O-trityl derivative 14 and by unambiguous synthesis from 6.
    DOI:
    10.1016/0008-6215(90)80136-q
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文献信息

  • CAPEK, KAREL;CADOVA, EVA;SEDMERA, PETR, CARBOHYDR. RES., 205,(1990) C. 161-171
    作者:CAPEK, KAREL、CADOVA, EVA、SEDMERA, PETR
    DOI:——
    日期:——
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