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3-O-cinnamyl-β-cyclodextrin | 869206-16-6

中文名称
——
中文别名
——
英文名称
3-O-cinnamyl-β-cyclodextrin
英文别名
——
3-O-cinnamyl-β-cyclodextrin化学式
CAS
869206-16-6
化学式
C51H78O35
mdl
——
分子量
1251.16
InChiKey
ZWHVJXCPROEVRZ-ZJSGGANXSA-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-O-cinnamyl-β-cyclodextrin臭氧 作用下, 以 甲醇 为溶剂, 反应 0.17h, 以94%的产率得到2-(β-cyclodextrin-3-O-yl)ethane-1-amine
    参考文献:
    名称:
    Flavin–cyclodextrin conjugates: effect of the structure on the catalytic activity in enantioselective sulfoxidations
    摘要:
    A series of flavin cyclodextrin conjugates has been prepared and tested in the enantioselective oxidations of prochiral aromatic and aliphatic sulfides with hydrogen peroxide. The newly prepared conjugates contain isoalloxazinium or alloxazinium moieties attached to the primary rim of alpha- and beta-cyclodextrins at the C-6 positions. In addition, flavinium units were attached to the secondary rim of the beta-cyclodextrin macrocycle. The relationship between the structural features and the catalytic performance of the conjugates, including those recently reported by us, was analyzed. The rate and enantioselectivity of the sulfoxidations catalyzed by flavin cyclodextrin conjugates are influenced mainly by the size of the cyclodextrin cavity, the type of flavin unit (alloxazine or isoalloxazine), and by the relative orientation of the flavin and cyclodextrin moieties. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2012.10.017
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