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methyl 2-acetamido-3,4-di-O-benzyl-2,7-dideoxy-7-(phenydimethylsilyl)-L-glycero-β-D-gluco-heptopyranoside | 352547-26-3

中文名称
——
中文别名
——
英文名称
methyl 2-acetamido-3,4-di-O-benzyl-2,7-dideoxy-7-(phenydimethylsilyl)-L-glycero-β-D-gluco-heptopyranoside
英文别名
N-[(2R,3R,4R,5S,6R)-6-[(1R)-2-[dimethyl(phenyl)silyl]-1-hydroxyethyl]-2-methoxy-4,5-bis(phenylmethoxy)oxan-3-yl]acetamide
methyl 2-acetamido-3,4-di-O-benzyl-2,7-dideoxy-7-(phenydimethylsilyl)-L-glycero-β-D-gluco-heptopyranoside化学式
CAS
352547-26-3
化学式
C32H41NO6Si
mdl
——
分子量
563.766
InChiKey
YAXPHBIHEQNFFG-YWTMIQCDSA-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):
    4.01
  • 重原子数:
    40
  • 可旋转键数:
    12
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    86.2
  • 氢给体数:
    2
  • 氢受体数:
    6

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-acetamido-3,4-di-O-benzyl-2,7-dideoxy-7-(phenydimethylsilyl)-L-glycero-β-D-gluco-heptopyranosidesodium acetate 、 potassium bromide 作用下, 以 溶剂黄146 为溶剂, 反应 2.0h, 以59%的产率得到methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-L-glycero-β-D-gluco-heptopyranoside
    参考文献:
    名称:
    Homologation of methyl 2-azido- and 2-acetamido-3,4-di-O-benzyl-2-deoxy-d-hexopyranosides with allyloxymethylmagnesium chloride
    摘要:
    Methyl 2-azido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha-, beta -D-gluco and alpha -D-manno configuration as well as methyl 2-acetamido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha- and beta -D-gluco configuration, protected at positions 3 and 4 with O-benzyl groups were reacted with an excess of allyloxymethylmagnesium or (phenyldimethylsilyl)methylmagnesium chlorides to afford mixtures of C-6 stereoisomeric heptopyranosides. Configuration of the products separated by column chromatography was assigned by H-1 NMR data. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(01)00078-7
  • 作为产物:
    参考文献:
    名称:
    Homologation of methyl 2-azido- and 2-acetamido-3,4-di-O-benzyl-2-deoxy-d-hexopyranosides with allyloxymethylmagnesium chloride
    摘要:
    Methyl 2-azido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha-, beta -D-gluco and alpha -D-manno configuration as well as methyl 2-acetamido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha- and beta -D-gluco configuration, protected at positions 3 and 4 with O-benzyl groups were reacted with an excess of allyloxymethylmagnesium or (phenyldimethylsilyl)methylmagnesium chlorides to afford mixtures of C-6 stereoisomeric heptopyranosides. Configuration of the products separated by column chromatography was assigned by H-1 NMR data. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(01)00078-7
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文献信息

  • Homologation of methyl 2-azido- and 2-acetamido-3,4-di-O-benzyl-2-deoxy-d-hexopyranosides with allyloxymethylmagnesium chloride
    作者:Barbara Grzeszczyk、Aleksander Zamojski
    DOI:10.1016/s0008-6215(01)00078-7
    日期:2001.5
    Methyl 2-azido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha-, beta -D-gluco and alpha -D-manno configuration as well as methyl 2-acetamido-2-deoxy-hexodialdo-1,5-pyranosides of the alpha- and beta -D-gluco configuration, protected at positions 3 and 4 with O-benzyl groups were reacted with an excess of allyloxymethylmagnesium or (phenyldimethylsilyl)methylmagnesium chlorides to afford mixtures of C-6 stereoisomeric heptopyranosides. Configuration of the products separated by column chromatography was assigned by H-1 NMR data. (C) 2001 Elsevier Science Ltd. All rights reserved.
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