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per-O-acetyl-per-6-azido-per-6-deoxy-3I-O-formylmethyl-β-cyclodextrin | 1415579-10-0

中文名称
——
中文别名
——
英文名称
per-O-acetyl-per-6-azido-per-6-deoxy-3I-O-formylmethyl-β-cyclodextrin
英文别名
——
per-O-acetyl-per-6-azido-per-6-deoxy-3<sup>I</sup>-O-formylmethyl-β-cyclodextrin化学式
CAS
1415579-10-0
化学式
C70H91N21O42
mdl
——
分子量
1898.61
InChiKey
VUUAKDZVWYVEHU-DCBUKTJTSA-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

  • 作为产物:
    描述:
    per-O-acetyl-per-6-azido-per-6-deoxy-3I-O-cinnamyl-β-cyclodextrin 在 臭氧 作用下, 以 甲醇氯仿 为溶剂, 反应 0.33h, 以67%的产率得到per-O-acetyl-per-6-azido-per-6-deoxy-3I-O-formylmethyl-β-cyclodextrin
    参考文献:
    名称:
    Synthesis of 3I-O and 2I-O-monosubstituted derivatives of per-6-azido-β-cyclodextrin—potential molecular scaffolds
    摘要:
    Alkylation of per-6-azido-beta-cyclodextrin by a suitable electrophilic reagent (cinnamyl bromide or propargyl bromide) gave a mixture of 3(I)-O and 2(I)-O regioisomers. After peracetylation and chromatographic separation on silica gel, pure isomers were isolated. Oxidative cleavage of cinnamyl double bond afforded the corresponding formylmethyl and carboxymethyl derivatives. The prepared scaffold molecules are equipped with two types of reactive groups which have a potential to serve as points of attachment for various compounds. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2012.09.003
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