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(1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol | 849065-24-3

中文名称
——
中文别名
——
英文名称
(1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol
英文别名
(1R,2R,5S)-2-Azido-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-ol;(1R,2R,5S)-2-azido-2-methyl-5-prop-1-en-2-ylcyclohexan-1-ol
(1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol化学式
CAS
849065-24-3
化学式
C10H17N3O
mdl
——
分子量
195.264
InChiKey
ZIRZULKNFAGGAD-IVZWLZJFSA-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):
    3.1
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    34.6
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol三苯基膦 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以77%的产率得到(1R,4S,6S)-4-isopropenyl-1-methyl-7-azabicyclo-[4.1.0]heptane
    参考文献:
    名称:
    A convenient synthesis of new diamine, amino alcohol and aminophosphines chiral auxiliaries based on limonene oxide
    摘要:
    A strategy for the synthesis of new chiral auxiliaries based upon vicinal diamines, amino alcohols and aminophosphines, obtained from limonene oxide, has been developed. The methodology allows the preparation of (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine starting from a commercially available mixture of cis/trans (4S)-(-)-limonene oxides, through a stereoconvergent synthetic sequence. The process starts from an inexpensive naturally occurring material, is amenable to scale-up and allows easy access to highly useful enantiopure building blocks and ligands, employed in asymmetric catalysis. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2009.08.012
  • 作为产物:
    描述:
    (−)-氧化柠檬烯(顺反异构体混合物) 在 sodium azide 、 氯化铵 作用下, 以 甲醇 为溶剂, 反应 24.0h, 生成 (1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol 、 (1R,2R,4S)-2-azido-1-methyl-4-(prop-1-en-2-yl)cyclohexanol
    参考文献:
    名称:
    Scaleable Syntheses of Isomeric Limonene Aziridines from the Commercially Available Mixture of cis- and trans-Limonene Oxides
    摘要:
    A short and efficient route to both isomers of limonene aziridine is described. The process is amenable to scale-up and allows easy access to multigram quantities of these highly useful chiral building blocks.
    DOI:
    10.1021/op0498464
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文献信息

  • Scaleable Syntheses of Isomeric Limonene Aziridines from the Commercially Available Mixture of <i>cis</i>- and <i>trans</i>-Limonene Oxides
    作者:Michael V. Voronkov、Alexander V. Gontcharov、Ramanaiah C. Kanamarlapudi、Paul F. Richardson、Zhi-Min Wang
    DOI:10.1021/op0498464
    日期:2005.3.1
    A short and efficient route to both isomers of limonene aziridine is described. The process is amenable to scale-up and allows easy access to multigram quantities of these highly useful chiral building blocks.
  • A convenient synthesis of new diamine, amino alcohol and aminophosphines chiral auxiliaries based on limonene oxide
    作者:Cristina Cimarelli、Davide Fratoni、Gianni Palmieri
    DOI:10.1016/j.tetasy.2009.08.012
    日期:2009.10
    A strategy for the synthesis of new chiral auxiliaries based upon vicinal diamines, amino alcohols and aminophosphines, obtained from limonene oxide, has been developed. The methodology allows the preparation of (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine starting from a commercially available mixture of cis/trans (4S)-(-)-limonene oxides, through a stereoconvergent synthetic sequence. The process starts from an inexpensive naturally occurring material, is amenable to scale-up and allows easy access to highly useful enantiopure building blocks and ligands, employed in asymmetric catalysis. (C) 2009 Elsevier Ltd. All rights reserved.
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