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prop-2-en-1-yl 2,3-di-O-benzoyl-4-O-[tert-butyl(dimethyl)silyl]-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside | 1419710-96-5

中文名称
——
中文别名
——
英文名称
prop-2-en-1-yl 2,3-di-O-benzoyl-4-O-[tert-butyl(dimethyl)silyl]-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
英文别名
——
prop-2-en-1-yl 2,3-di-O-benzoyl-4-O-[tert-butyl(dimethyl)silyl]-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside化学式
CAS
1419710-96-5
化学式
C81H90N2O27Si
mdl
——
分子量
1551.69
InChiKey
IVCURVOTGZJAQZ-NCASYQSESA-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

反应信息

  • 作为反应物:
    描述:
    prop-2-en-1-yl 2,3-di-O-benzoyl-4-O-[tert-butyl(dimethyl)silyl]-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside氟化氢吡啶 作用下, 以 四氢呋喃 为溶剂, 反应 96.0h, 以46%的产率得到prop-2-en-1-yl 2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-2-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of 13C-labeled and functionalized Hyaluronan derivatives for biophysical studies and surface modifications
    摘要:
    A convergent synthesis of a tetrasaccharide partial sequence of C-13-labeled Hyaluronan is presented. This tetrasaccharide can be used for biophysical studies as well as for surface modifications. Furthermore, tetrasaccharide 7 can be employed for the synthesis of additionally labeled higher oligomers of Hyaluronan on the basis of the presented methodology. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2012.11.025
  • 作为产物:
    描述:
    乙酸酐吡啶 为溶剂, 反应 16.0h, 以77.3 mg的产率得到prop-2-en-1-yl 2,3-di-O-benzoyl-4-O-[tert-butyl(dimethyl)silyl]-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl-(1→4)-2,3-di-O-benzoyl-6-methyl-β-D-glucopyranuronosyl-(1→3)-2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
    参考文献:
    名称:
    Synthesis of 13C-labeled and functionalized Hyaluronan derivatives for biophysical studies and surface modifications
    摘要:
    A convergent synthesis of a tetrasaccharide partial sequence of C-13-labeled Hyaluronan is presented. This tetrasaccharide can be used for biophysical studies as well as for surface modifications. Furthermore, tetrasaccharide 7 can be employed for the synthesis of additionally labeled higher oligomers of Hyaluronan on the basis of the presented methodology. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2012.11.025
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