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| 1239956-29-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1239956-29-6
化学式
C27H28N6O8
mdl
——
分子量
564.555
InChiKey
MVZVTQIZLIRUHO-YMGHBJPRSA-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:
    2,2-二甲氧基丙烷 在 BSA 作用下, 以 丙酮 为溶剂, 以37%的产率得到1-[(3aR,4R,6R,6aR)-6-[(1S,2R)-2-azido-3-(2,3-dihydroindol-1-yl)-1-hydroxy-3-oxopropyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]-3-[(4-methoxyphenyl)methyl]pyrimidine-2,4-dione
    参考文献:
    名称:
    Efficient synthesis of the core structure of muraymycin and caprazamycin nucleoside antibiotics based on a stereochemically revised sulfur ylide reaction
    摘要:
    The reaction of protected uridine 5'-aldehydes with sulfur ylides has been reinvestigated Further transformation of the resulting epoxide product provided a compound of which a single crystal for X-ray diffraction was obtained. As a consequence from the elucidated structure, the stereochemical configuration of the epoxide furnished by the sulfur ylide reaction was revised. Based on these results, an efficient synthesis of the core structure of the naturally occurring muraymycin and caprazamycin nucleoside antibiotics was developed. (C) 2010 Elsevier Ltd. All rights reserved
    DOI:
    10.1016/j.tetasy.2010.03.037
  • 作为产物:
    描述:
    乙酰氯 作用下, 以 甲醇 为溶剂, 以90%的产率得到
    参考文献:
    名称:
    Efficient synthesis of the core structure of muraymycin and caprazamycin nucleoside antibiotics based on a stereochemically revised sulfur ylide reaction
    摘要:
    The reaction of protected uridine 5'-aldehydes with sulfur ylides has been reinvestigated Further transformation of the resulting epoxide product provided a compound of which a single crystal for X-ray diffraction was obtained. As a consequence from the elucidated structure, the stereochemical configuration of the epoxide furnished by the sulfur ylide reaction was revised. Based on these results, an efficient synthesis of the core structure of the naturally occurring muraymycin and caprazamycin nucleoside antibiotics was developed. (C) 2010 Elsevier Ltd. All rights reserved
    DOI:
    10.1016/j.tetasy.2010.03.037
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