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2,4-dinitro-6-(methoxycarbonyl)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-α-D-glucopyranoside | 853014-82-1

中文名称
——
中文别名
——
英文名称
2,4-dinitro-6-(methoxycarbonyl)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-α-D-glucopyranoside
英文别名
methyl 2-[(2R,3R,4R,5S,6R)-4,5-diacetyloxy-6-(acetyloxymethyl)-3-[(2,2,2-trifluoroacetyl)amino]oxan-2-yl]oxy-3,5-dinitrobenzoate
2,4-dinitro-6-(methoxycarbonyl)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-α-D-glucopyranoside化学式
CAS
853014-82-1
化学式
C22H22F3N3O15
mdl
——
分子量
625.423
InChiKey
FTXXFERIVRDJAH-FEBARNBZSA-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):
    1.6
  • 重原子数:
    43
  • 可旋转键数:
    12
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    244
  • 氢给体数:
    1
  • 氢受体数:
    18

反应信息

  • 作为反应物:
    描述:
    2,4-dinitro-6-(methoxycarbonyl)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-α-D-glucopyranoside双丙酮半乳糖N-甲基吡咯烷酮 为溶剂, 反应 40.0h, 以45%的产率得到3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-β-D-glucopyranosyl-(1->6)-(1,2:3,4)-di-O-isopropylidene-α-D-galactopyranose
    参考文献:
    名称:
    Glucosamine derived DISAL donors for stereoselective glycosylations under neutral conditions
    摘要:
    DISAL (methyl 3,5-dinitrosa/icylate) D-glcosyl, D-galactosyl, D-mannosyl, and L-quinovosyl donors have previously provided the efficient glycosylation of a range of substrates under either strictly neutral, mildly basic, or very mildly Lewis acidic (LiClO4) conditions. Herein we report the synthesis of new glucosamine DISAL donors, carrying N-TCP, -Troc, or -TFAc protecting groups, and their use in beta-(1,2-trans) selective glycosylations, primarily in NMP in the absence of any added Lewis acids, or in CH3NO2 with LiClO4. Finally, precise microwave heating proved effective in promoting the difficult glycosylation of the 3-OH of a glucosamine derivative. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2005.02.029
  • 作为产物:
    描述:
    3,4,6-Tri-O-acetyl-2-trifluoracetamino-2-desoxy-D-glucose 、 methyl 2-fluoro-3,5-dinitrobenzoic ester4-二甲氨基吡啶lithium carbonate 作用下, 以 二氯甲烷 为溶剂, 反应 1.5h, 以87%的产率得到2,4-dinitro-6-(methoxycarbonyl)phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-(trifluoroacetamido)-α-D-glucopyranoside
    参考文献:
    名称:
    Glucosamine derived DISAL donors for stereoselective glycosylations under neutral conditions
    摘要:
    DISAL (methyl 3,5-dinitrosa/icylate) D-glcosyl, D-galactosyl, D-mannosyl, and L-quinovosyl donors have previously provided the efficient glycosylation of a range of substrates under either strictly neutral, mildly basic, or very mildly Lewis acidic (LiClO4) conditions. Herein we report the synthesis of new glucosamine DISAL donors, carrying N-TCP, -Troc, or -TFAc protecting groups, and their use in beta-(1,2-trans) selective glycosylations, primarily in NMP in the absence of any added Lewis acids, or in CH3NO2 with LiClO4. Finally, precise microwave heating proved effective in promoting the difficult glycosylation of the 3-OH of a glucosamine derivative. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2005.02.029
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