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tert-butyl (2R,6S)-2-(benzenesulfonylmethyl)-6-methylpiperidine-1-carboxylate | 192133-22-5

中文名称
——
中文别名
——
英文名称
tert-butyl (2R,6S)-2-(benzenesulfonylmethyl)-6-methylpiperidine-1-carboxylate
英文别名
——
tert-butyl (2R,6S)-2-(benzenesulfonylmethyl)-6-methylpiperidine-1-carboxylate化学式
CAS
192133-22-5
化学式
C18H27NO4S
mdl
——
分子量
353.483
InChiKey
DWIGIUUWFVJLJT-LSDHHAIUSA-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):
    3.4
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    72.1
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    tert-butyl (2R,6S)-2-(benzenesulfonylmethyl)-6-methylpiperidine-1-carboxylate三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以4.91 g的产率得到(2R,6S)-2-Benzenesulfonylmethyl-6-methyl-piperidine
    参考文献:
    名称:
    Applications of Organosulfur Chemistry to Organic Synthesis:  Total Synthesis of (+)-Himbeline and (+)-Himbacine
    摘要:
    Total syntheses of(+)-himbacine (1) and (+)-himbeline (2) are described. The synthesis involves the preparation of sulfone 38 and aldehyde 42 as single enantiomers followed by coupling of these compounds using a Julia-Lythgoe olefination. The preparation of sulfone 38 features an acid-promoted intramolecular Diels-Alder reaction of an alpha,beta-unsaturated thioester while the synthesis of 42 features a Beak, alkylation of piperidine 39.
    DOI:
    10.1021/jo970612a
  • 作为产物:
    参考文献:
    名称:
    Applications of Organosulfur Chemistry to Organic Synthesis:  Total Synthesis of (+)-Himbeline and (+)-Himbacine
    摘要:
    Total syntheses of(+)-himbacine (1) and (+)-himbeline (2) are described. The synthesis involves the preparation of sulfone 38 and aldehyde 42 as single enantiomers followed by coupling of these compounds using a Julia-Lythgoe olefination. The preparation of sulfone 38 features an acid-promoted intramolecular Diels-Alder reaction of an alpha,beta-unsaturated thioester while the synthesis of 42 features a Beak, alkylation of piperidine 39.
    DOI:
    10.1021/jo970612a
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文献信息

  • Applications of Organosulfur Chemistry to Organic Synthesis:  Total Synthesis of (+)-Himbeline and (+)-Himbacine
    作者:David J. Hart、Jing Li、Wen-Lian Wu、Alan P. Kozikowski
    DOI:10.1021/jo970612a
    日期:1997.7.1
    Total syntheses of(+)-himbacine (1) and (+)-himbeline (2) are described. The synthesis involves the preparation of sulfone 38 and aldehyde 42 as single enantiomers followed by coupling of these compounds using a Julia-Lythgoe olefination. The preparation of sulfone 38 features an acid-promoted intramolecular Diels-Alder reaction of an alpha,beta-unsaturated thioester while the synthesis of 42 features a Beak, alkylation of piperidine 39.
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