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(2-methoxyphenyl)-dimethyl-[(2R,3R,4S,5R,6R)-2-pent-4-enoxy-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]oxysilane | 616239-49-7

中文名称
——
中文别名
——
英文名称
(2-methoxyphenyl)-dimethyl-[(2R,3R,4S,5R,6R)-2-pent-4-enoxy-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]oxysilane
英文别名
——
(2-methoxyphenyl)-dimethyl-[(2R,3R,4S,5R,6R)-2-pent-4-enoxy-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]oxysilane化学式
CAS
616239-49-7
化学式
C41H50O7Si
mdl
——
分子量
682.929
InChiKey
TVIWCBKQHDZDAR-HXBMFNGISA-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):
    7.59
  • 重原子数:
    49
  • 可旋转键数:
    19
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    64.6
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    (2-methoxyphenyl)-dimethyl-[(2R,3R,4S,5R,6R)-2-pent-4-enoxy-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]oxysilane iodonium di(2,4,6-trimethylpyridine) perchlorate 、 4 A molecular sieve 、 氢气 作用下, 以 二氯甲烷 为溶剂, 反应 6.0h, 生成 (2R,3S,4R,5R,6R)-2-Hydroxymethyl-6-(2-methoxy-phenyl)-tetrahydro-pyran-3,4,5-triol
    参考文献:
    名称:
    Stereodirected Synthesis of Aryl α-C-Glycosides from 2-O-Arylsilyl-glucopyranosides
    摘要:
    An efficient procedure for the stereoselective synthesis of aryl (x-C-glycosides is presented. The key step of the method is the intramolecular delivery of the aryl group from a 2-O-aryldialkylsilyl substituent to the anomeric carbon by an electrophilic ipso-desilylation; this process leads exclusively to the product having the 1,2-cis configuration.
    DOI:
    10.1021/ol035529q
  • 作为产物:
    描述:
    4-pentenyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside 在 正丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 3.25h, 生成 (2-methoxyphenyl)-dimethyl-[(2R,3R,4S,5R,6R)-2-pent-4-enoxy-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]oxysilane
    参考文献:
    名称:
    Stereodirected Synthesis of Aryl α-C-Glycosides from 2-O-Arylsilyl-glucopyranosides
    摘要:
    An efficient procedure for the stereoselective synthesis of aryl (x-C-glycosides is presented. The key step of the method is the intramolecular delivery of the aryl group from a 2-O-aryldialkylsilyl substituent to the anomeric carbon by an electrophilic ipso-desilylation; this process leads exclusively to the product having the 1,2-cis configuration.
    DOI:
    10.1021/ol035529q
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文献信息

  • Stereodirected Synthesis of Aryl α-<i>C</i>-Glycosides from 2-<i>O</i>-Arylsilyl-glucopyranosides
    作者:Cyril Rousseau、Olivier R. Martin
    DOI:10.1021/ol035529q
    日期:2003.10.1
    An efficient procedure for the stereoselective synthesis of aryl (x-C-glycosides is presented. The key step of the method is the intramolecular delivery of the aryl group from a 2-O-aryldialkylsilyl substituent to the anomeric carbon by an electrophilic ipso-desilylation; this process leads exclusively to the product having the 1,2-cis configuration.
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