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(1S,3R,4S,5R,6S)-1-amino-3-(2,2-dimethylpent-4-enylamino)-7-oxaspiro[5.6]dodec-9-ene-4,5-diol | 1261084-77-8

中文名称
——
中文别名
——
英文名称
(1S,3R,4S,5R,6S)-1-amino-3-(2,2-dimethylpent-4-enylamino)-7-oxaspiro[5.6]dodec-9-ene-4,5-diol
英文别名
——
(1S,3R,4S,5R,6S)-1-amino-3-(2,2-dimethylpent-4-enylamino)-7-oxaspiro[5.6]dodec-9-ene-4,5-diol化学式
CAS
1261084-77-8
化学式
C18H32N2O3
mdl
——
分子量
324.464
InChiKey
DMJPZNSQIMFJNQ-JFBPSJKJSA-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):
    1
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    87.7
  • 氢给体数:
    4
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    、 potassium hydroxide 作用下, 以 甲醇 为溶剂, 反应 12.0h, 以78%的产率得到(1S,3R,4S,5R,6S)-1-amino-3-(2,2-dimethylpent-4-enylamino)-7-oxaspiro[5.6]dodec-9-ene-4,5-diol
    参考文献:
    名称:
    Second generation analogs of rigid 6,7-spiro scaffolds targeting the bacterial ribosome
    摘要:
    Previous work from our group described the synthesis and biological evaluation of new rigid, 6,6- and 6,7-spiro aminoglycosidic scaffolds targeting the bacterial ribosome. Herein we describe an improved synthetic protocol for their construction, and extend our study by further amino-functionalization of their 6,7-spiro analogs. The synthetic strategy, preparation and evaluation of some representative examples are reported. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.10.001
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文献信息

  • Second generation analogs of rigid 6,7-spiro scaffolds targeting the bacterial ribosome
    作者:Christos I. Stathakis、Ioannis Mavridis、Georgia Kythreoti、Athanasios Papakyriakou、Ioannis A. Katsoulis、Thomas Cottin、Panoula Anastasopoulou、Dionisios Vourloumis
    DOI:10.1016/j.bmcl.2010.10.001
    日期:2010.12
    Previous work from our group described the synthesis and biological evaluation of new rigid, 6,6- and 6,7-spiro aminoglycosidic scaffolds targeting the bacterial ribosome. Herein we describe an improved synthetic protocol for their construction, and extend our study by further amino-functionalization of their 6,7-spiro analogs. The synthetic strategy, preparation and evaluation of some representative examples are reported. (C) 2010 Elsevier Ltd. All rights reserved.
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