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methyl 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-1-thio-β-L-galacto-decopyranoside | 408497-02-9

中文名称
——
中文别名
——
英文名称
methyl 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-1-thio-β-L-galacto-decopyranoside
英文别名
(2R,3S,4R,5R,6S)-2-methylsulfanyl-6-pentyl-3,4,5-tris(phenylmethoxy)oxane
methyl 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-1-thio-β-L-galacto-decopyranoside化学式
CAS
408497-02-9
化学式
C32H40O4S
mdl
——
分子量
520.733
InChiKey
XGABIZMMGYMQFK-CNLJACSDSA-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):
    7.3
  • 重原子数:
    37
  • 可旋转键数:
    14
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    62.2
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    methyl 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-1-thio-β-L-galacto-decopyranoside 在 iodonium(di-γ-collidine) perchlorate 、 4 A molecular sieve 、 sodium methylate溶剂黄146 作用下, 以 甲醇乙醚二氯甲烷 为溶剂, 反应 7.5h, 生成 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-α-L-galacto-decopyranosyl-(1->2)-β-D-galactopyranosyl-(1->4)-α-D-glucopyranose
    参考文献:
    名称:
    SYNTHESIS AND APPLICATION OF SPACER-MODIFIED L-FUCOSE ANALOGUES1
    摘要:
    Starting from 6-O-tert-butyldimethylsilyl-2,3;4,5-di-O-isopropylidenealdehydo-D-galactose (1), the carbon backbone elongated GDP-L-fucose analogue 15 bearing a chromophore tag at the end of a spacer was synthesized. Additionally, the analogues of 3-L-fucosyllactose (29) and 2'-L-fucosyllactose (36), where the fucosyl moiety is marked by a five atom alkyl chain at C-5, were prepared as labeled oligosaccharides of human milk.
    DOI:
    10.1081/car-100108277
  • 作为产物:
    描述:
    1,2,3,4-tetra-O-acetyl-6,7,8,9,10-pentadeoxy-L-galacto-decopyranose 在 三氟甲磺酸三甲基硅酯sodium methylate 、 sodium hydride 作用下, 以 甲醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 生成 methyl 2,3,4-tri-O-benzyl-6,7,8,9,10-pentadeoxy-1-thio-β-L-galacto-decopyranoside
    参考文献:
    名称:
    SYNTHESIS AND APPLICATION OF SPACER-MODIFIED L-FUCOSE ANALOGUES1
    摘要:
    Starting from 6-O-tert-butyldimethylsilyl-2,3;4,5-di-O-isopropylidenealdehydo-D-galactose (1), the carbon backbone elongated GDP-L-fucose analogue 15 bearing a chromophore tag at the end of a spacer was synthesized. Additionally, the analogues of 3-L-fucosyllactose (29) and 2'-L-fucosyllactose (36), where the fucosyl moiety is marked by a five atom alkyl chain at C-5, were prepared as labeled oligosaccharides of human milk.
    DOI:
    10.1081/car-100108277
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文献信息

  • SYNTHESIS AND APPLICATION OF SPACER-MODIFIED L-FUCOSE ANALOGUES1
    作者:Andrej-Jakob Ott、Meinolf Brackhagen、Anahit Davtyan、Birte Nolting、Hanna Boye、Astrid Schoknecht、Christian Vogel
    DOI:10.1081/car-100108277
    日期:——
    Starting from 6-O-tert-butyldimethylsilyl-2,3;4,5-di-O-isopropylidenealdehydo-D-galactose (1), the carbon backbone elongated GDP-L-fucose analogue 15 bearing a chromophore tag at the end of a spacer was synthesized. Additionally, the analogues of 3-L-fucosyllactose (29) and 2'-L-fucosyllactose (36), where the fucosyl moiety is marked by a five atom alkyl chain at C-5, were prepared as labeled oligosaccharides of human milk.
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