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(3R, 8aS)-hexahydro-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazin-5-one | 1399859-36-9

中文名称
——
中文别名
——
英文名称
(3R, 8aS)-hexahydro-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazin-5-one
英文别名
——
(3R, 8aS)-hexahydro-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazin-5-one化学式
CAS
1399859-36-9
化学式
C19H20N2O2
mdl
——
分子量
308.38
InChiKey
LZJLGQRZCMSHRD-PKOBYXMFSA-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:
    (3R, 8aS)-hexahydro-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazin-5-one 在 aluminum (III) chloride 、 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Stereoselective synthesis of enantiopure N-protected-3-arylpiperazines from keto-esters
    摘要:
    An efficient method for a stereoselective synthesis of optically pure N-Boc-3-arylpiperazines has been developed. After optimization of the protecting group strategy and experimental conditions, compounds were obtained via a highly stereoselective synthesis in up to 45% overall yield. This is a practical route to optically pure piperazines for medicinal chemistry. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.07.031
  • 作为产物:
    描述:
    (3R, 8aS)-benzylhexahydro-5-oxo-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazine-7-carboxylate 在 20% Pd/C 、 氢气 作用下, 以 乙醇 为溶剂, 反应 20.0h, 以92%的产率得到(3R, 8aS)-hexahydro-3-phenyl-8a-p-tolyoxazolo[3,2-a]pyrazin-5-one
    参考文献:
    名称:
    Stereoselective synthesis of enantiopure N-protected-3-arylpiperazines from keto-esters
    摘要:
    An efficient method for a stereoselective synthesis of optically pure N-Boc-3-arylpiperazines has been developed. After optimization of the protecting group strategy and experimental conditions, compounds were obtained via a highly stereoselective synthesis in up to 45% overall yield. This is a practical route to optically pure piperazines for medicinal chemistry. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.07.031
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