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2-cyanoethyl-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-N,N'-diisopropylphosphoramidite | 1085304-09-1

中文名称
——
中文别名
——
英文名称
2-cyanoethyl-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-N,N'-diisopropylphosphoramidite
英文别名
Bn(-2)[Bn(-3)][Bn(-4)][Bn(-6)]Glc(a)-O-P(OCH2CH2CN)N(iPr)2;3-[[di(propan-2-yl)amino]-[(2R,3R,4S,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]oxyphosphanyl]oxypropanenitrile
2-cyanoethyl-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-N,N'-diisopropylphosphoramidite化学式
CAS
1085304-09-1
化学式
C43H53N2O7P
mdl
——
分子量
740.877
InChiKey
AMYJWKNFCAPSPN-DUBFABQZSA-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
  • 重原子数:
    53
  • 可旋转键数:
    21
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    91.6
  • 氢给体数:
    0
  • 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:
    2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl iodide 、 (iPr2N)2PO(CH2)2CN1,8-双二甲氨基萘 作用下, 以 甲苯 为溶剂, 反应 48.0h, 以73%的产率得到2-cyanoethyl-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-N,N'-diisopropylphosphoramidite
    参考文献:
    名称:
    Stereoselective Synthesis of α-Glycosyl Phosphites and Phosphoramidites via O-Selective Glycosylation of H-Phosphonate Derivatives
    摘要:
    A highly stereo- and chemoselective glycosylation of H-phosphonate derivatives with glycosyl iodides was discovered as a reverse reaction of the formation of a glycosyl iodide from a glycosyl phosphite and I- under mild acidic conditions. Further study on the unique reaction showed that the reaction provided various alpha-glycosyl phosphites; and phosphoramidites in a highly stereoselective manner with complete O-selectivity.
    DOI:
    10.1021/ol802190x
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文献信息

  • Stereoselective Synthesis of α-Glycosyl Phosphites and Phosphoramidites via <i>O</i>-Selective Glycosylation of <i>H</i>-Phosphonate Derivatives
    作者:Fumiko Matsumura、Natsuhisa Oka、Takeshi Wada
    DOI:10.1021/ol802190x
    日期:2008.11.20
    A highly stereo- and chemoselective glycosylation of H-phosphonate derivatives with glycosyl iodides was discovered as a reverse reaction of the formation of a glycosyl iodide from a glycosyl phosphite and I- under mild acidic conditions. Further study on the unique reaction showed that the reaction provided various alpha-glycosyl phosphites; and phosphoramidites in a highly stereoselective manner with complete O-selectivity.
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