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3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-glycero-D-gluco-D-gluco-tridecadialdo-7-en-1,5-pyranoside | 389885-59-0

中文名称
——
中文别名
——
英文名称
3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-glycero-D-gluco-D-gluco-tridecadialdo-7-en-1,5-pyranoside
英文别名
——
3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-glycero-D-gluco-D-gluco-tridecadialdo-7-en-1,5-pyranoside化学式
CAS
389885-59-0
化学式
C84H96O17Si
mdl
——
分子量
1405.76
InChiKey
FODWCRYXFUHYGH-FSWYEJIUSA-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:
    3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-glycero-D-gluco-D-gluco-tridecadialdo-7-en-1,5-pyranoside臭氧 、 sodium tetrahydroborate 作用下, 以 甲醇二氯甲烷 为溶剂, 以68%的产率得到3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-D-glycero-α-D-glucopyranoside
    参考文献:
    名称:
    REACTION OF SUGAR PHOSPHONATES WITH SUCROSE ALDEHYDES. SYNTHESIS OF HIGHER ANALOGS OF SUCROSE
    摘要:
    The Horner-Emmons reaction between sugar phosphonates Sug-C(O)CH2 P(O)(OMe)(2) and aldehydes derived from sucrose afforded precursors of higher analogs of the general formula Sug-C(O)CH==CH-Suc. An example of the functionalization of the internal three-carbon saccharide connecting unit is provided.
    DOI:
    10.1081/car-100105713
  • 作为产物:
    描述:
    3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-galacto-D-gluco-tridecadialdo-7-en-6-ulo-1,5-pyranoside 在 zinc borohydride 作用下, 以 乙醚 为溶剂, 以83%的产率得到3,4-di-O-benzyl-1-O-benzyloxymethyl-6-O-t-butyldiphenylsilyl-β-D-fructofuranosyl-(2-1)-(E)-2,3,4-tri-O-benzyl-7,8-dideoxy-10,11:12,13-di-O-isopropylidene-β-L-glycero-D-gluco-D-gluco-tridecadialdo-7-en-1,5-pyranoside
    参考文献:
    名称:
    REACTION OF SUGAR PHOSPHONATES WITH SUCROSE ALDEHYDES. SYNTHESIS OF HIGHER ANALOGS OF SUCROSE
    摘要:
    The Horner-Emmons reaction between sugar phosphonates Sug-C(O)CH2 P(O)(OMe)(2) and aldehydes derived from sucrose afforded precursors of higher analogs of the general formula Sug-C(O)CH==CH-Suc. An example of the functionalization of the internal three-carbon saccharide connecting unit is provided.
    DOI:
    10.1081/car-100105713
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