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(1S,3R,5R)-3-butyl-5-propylthiomorpholine-1-oxide | 1451261-05-4

中文名称
——
中文别名
——
英文名称
(1S,3R,5R)-3-butyl-5-propylthiomorpholine-1-oxide
英文别名
(1S,3R,5R)-3-butyl-5-propyl-1,4-thiazinane 1-oxide
(1S,3R,5R)-3-butyl-5-propylthiomorpholine-1-oxide化学式
CAS
1451261-05-4
化学式
C11H23NOS
mdl
——
分子量
217.376
InChiKey
ZSGAFOHYCGFXFP-GYSYKLTISA-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):
    1.8
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    48.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (1S,3R,5R)-3-butyl-5-propylthiomorpholine-1-oxide间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Stereodivergent Access to Cis- and Trans-3,5-Disubstituted 1,4-Thiazane 1-Oxides by Cyclization of Homochiral β-Amino Sulfoxides and Sulfones. The Preparation of Isomeric Ant Venom Alkaloids
    摘要:
    Intramolecular conjugate additions of homochiral (E)-1-alkenyl 2-aminoalkyl sulfoxides and sulfones were investigated. The relative position of the 3,5-substituents of the resulting 1,4-thiazane oxides was found to be dependent on the oxidation state of the sulfur atom, demonstrating a simple and highly stereodivergent synthetic protocol. Selected cis- and trans-3,5-disubstituted 1,4-thiazane dioxides were converted to cis- and trans-2,5-disubstituted pyrrolidines, known ant venom alkaloids.
    DOI:
    10.1021/ol4023003
  • 作为产物:
    描述:
    (SS,2R)-1-((E)-1-hexenylsulfinyl)pentan-2-amine三乙胺 作用下, 以 甲醇 为溶剂, 反应 8.0h, 以96%的产率得到(1S,3R,5R)-3-butyl-5-propylthiomorpholine-1-oxide
    参考文献:
    名称:
    Stereodivergent Access to Cis- and Trans-3,5-Disubstituted 1,4-Thiazane 1-Oxides by Cyclization of Homochiral β-Amino Sulfoxides and Sulfones. The Preparation of Isomeric Ant Venom Alkaloids
    摘要:
    Intramolecular conjugate additions of homochiral (E)-1-alkenyl 2-aminoalkyl sulfoxides and sulfones were investigated. The relative position of the 3,5-substituents of the resulting 1,4-thiazane oxides was found to be dependent on the oxidation state of the sulfur atom, demonstrating a simple and highly stereodivergent synthetic protocol. Selected cis- and trans-3,5-disubstituted 1,4-thiazane dioxides were converted to cis- and trans-2,5-disubstituted pyrrolidines, known ant venom alkaloids.
    DOI:
    10.1021/ol4023003
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