摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(10S)-3β,17β-dihydroxy-5,10-secoandrostan-5-one | 929718-29-6

中文名称
——
中文别名
——
英文名称
(10S)-3β,17β-dihydroxy-5,10-secoandrostan-5-one
英文别名
——
(10S)-3β,17β-dihydroxy-5,10-secoandrostan-5-one化学式
CAS
929718-29-6
化学式
C19H32O3
mdl
——
分子量
308.461
InChiKey
JMCYIUUDKBVHGN-FNXQGGOISA-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:
    (10S)-3β,17β-dihydroxy-5,10-secoandrostan-5-one对甲苯磺酸 作用下, 以 氯仿 为溶剂, 反应 0.67h, 以48%的产率得到(3Z,10S)-17β-hydroxy-5,10-secoandrost-3-en-5-one
    参考文献:
    名称:
    Isolation and structure elucidation of new radical oxidation products of 5-hydroxy steroids
    摘要:
    Three new products have been isolated from the lead-tetraacetate version of the hypoiodite oxidation of 3 beta,17 beta-diacetoxy-5-hydroxy-5 alpha-androstane. Along with the expected 1(10)unsaturated 5,10-seco steroidal 5-ketones, the fragmentation reaction gave two epimeric C-4 iodides. Their structural assignment was based on X-ray data of one of them ((4R,10S)-4iodo-3 beta,17 beta-diacetoxy-5,10-secoandrostan-5-one). The third new product was found to be the 5 beta,6 beta-epoxide resulting from the dehydration of the tertiary alcohol followed by epoxidation of the intermediate Delta(5)-olefin. (c) 2006 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2006.01.008
  • 作为产物:
    描述:
    (10S)-3β,17β-diacetoxy-5,10-secoandrostan-5-one氢氧化钾 作用下, 以 甲醇 为溶剂, 反应 0.67h, 以72%的产率得到(10S)-3β,17β-dihydroxy-5,10-secoandrostan-5-one
    参考文献:
    名称:
    Isolation and structure elucidation of new radical oxidation products of 5-hydroxy steroids
    摘要:
    Three new products have been isolated from the lead-tetraacetate version of the hypoiodite oxidation of 3 beta,17 beta-diacetoxy-5-hydroxy-5 alpha-androstane. Along with the expected 1(10)unsaturated 5,10-seco steroidal 5-ketones, the fragmentation reaction gave two epimeric C-4 iodides. Their structural assignment was based on X-ray data of one of them ((4R,10S)-4iodo-3 beta,17 beta-diacetoxy-5,10-secoandrostan-5-one). The third new product was found to be the 5 beta,6 beta-epoxide resulting from the dehydration of the tertiary alcohol followed by epoxidation of the intermediate Delta(5)-olefin. (c) 2006 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2006.01.008
点击查看最新优质反应信息