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benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside | 1133161-70-2

中文名称
——
中文别名
——
英文名称
benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside
英文别名
[(2R,3S,4S,5R,6S)-4-hydroxy-6-[(2S,3S,4R,5R,6R)-4-hydroxy-5-iodo-2,4-dimethyl-6-phenylmethoxyoxan-3-yl]oxy-2-methyl-5-(4-methylphenyl)sulfanyloxan-3-yl] benzoate
benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside化学式
CAS
1133161-70-2
化学式
C34H39IO8S
mdl
——
分子量
734.649
InChiKey
ITAQHXNOQCQXKS-UVAMDTGHSA-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):
    6.1
  • 重原子数:
    44
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    129
  • 氢给体数:
    2
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    benzyl 2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranosidep-tolyl 2,3-anhydro-4-O-benzoyl-1-thio-α-D-rhamnopyranoside 在 copper(II) bis(trifluoromethanesulfonate) 作用下, 以 二氯甲烷 为溶剂, 生成 benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside 、 benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->3)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside
    参考文献:
    名称:
    2,3-Anhydrosugars in Glycoside Bond Synthesis. Application to 2,6-Dideoxypyranosides
    摘要:
    We describe here the first use of 2,3-anhydrosugars as glycosylating agents for the preparation of 2-deoxypyranosides. In particular, the methodology was used to assemble 2,6-dideoxysugar glycosides. Glycosylation of a panel of alcohols with one of two 6-deoxy-2,3-anhydrosugar thioglycosides (8 and 9) in the presence of a Lewis acid afforded 2,6-dideoxy-2-thiotolyl glycoside products in generally excellent yields with an exclusively syn relationship between the aglycon and the C-3 hydroxyl group. Removal of the 2-thiotolyl group can be achieved upon reaction with tri-n-butyltin hydride and AIBN to give the corresponding 2,6-dideoxy pyranosides. Once developed, the method was applied to the synthesis of oligosaccharide moieties in the natural products apoptolidin and olivomycin A.
    DOI:
    10.1021/jo900131a
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