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5β,17β-dihydroxyandrostan-3-one | 121145-41-3

中文名称
——
中文别名
——
英文名称
5β,17β-dihydroxyandrostan-3-one
英文别名
(5S,8S,9S,10R,13S,14S,17S)-5,17-dihydroxy-10,13-dimethyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
5β,17β-dihydroxyandrostan-3-one化学式
CAS
121145-41-3
化学式
C19H30O3
mdl
——
分子量
306.445
InChiKey
OOFHIFZCMQKEBH-WRYXYBQESA-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):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    5β,17β-dihydroxyandrostan-3-one 生成 3-Oxo-5β-hydroxy-17β-acetoxy-androstan
    参考文献:
    名称:
    HOLLAND, HERBERT L.;BROWN, FRANCES M.;CHENCHAIAHI, P. CHINNA;CHERNISHENKO+, CAN. J. CHEM., 67,(1989) N, C. 268-274
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    Bell,A.M. et al., Journal of the Chemical Society. Perkin transactions I, 1973, p. 2131 - 2136
    摘要:
    DOI:
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文献信息

  • The organoselenium-mediated reduction of α,β-epoxy ketones, α,β-epoxy esters, and their congeners to β-hydroxy carbonyl compounds: Novel methodologies for the synthesis of aldols and their analogues
    作者:Masaaki Miyashita、Toshio Suzuki、Masahide Hoshino、Akira Yoshikoshi
    DOI:10.1016/s0040-4020(97)00781-3
    日期:1997.9
    Novel methods for the reduction of α,β-epoxy ketones, α,β-epoxy esters (glycidic esters), and their congeners to β-hydroxy carbonyl compounds (aldols) by the use of organoselenium reagents are described. The reagents, a sodium phenylseleno(triethyl)borate complex Na[PhSeB(OEt)3] easily prepared by reduction of (PhSe)2 with NaBH4 in EtOH and benzeneselenol (PhSeH) generated in situ from the borate complex
    描述了通过使用有机硒试剂将α,β-环氧酮,α,β-环氧酯(缩水甘油酯)及其同类物还原为β-羟基羰基化合物(醛醇)的新方法。通过在EtOH中用NaBH 4还原(PhSe)2和原位生成的苯硒酚(PhSeH),可以轻松制备苯基硒基(三乙基)硼酸钠复合物Na [PhSeB(OEt)3 ]通过添加乙酸从硼酸盐配合物中得到的氯已被证明可作为这些转化的极好的还原剂。有机硒介导的α,β-环氧羰基化合物在α-碳上区域特异性还原,从而以优异的收率生产出多种环状(分子内)醇醛和非环状(分子间)醇醛。定量机理研究表明,与常见的电子转移还原剂相比,有机硒介导的还原通过α取代过程进行。
  • Lithium naphthalenide induced reductive cleavage of α,β-epoxy ketones: an efficient procedure for the preparation of β-hydroxy ketones
    作者:Renata Jankowska、Hsing-Jang Liu、George L. Mhehe
    DOI:10.1039/a904646a
    日期:——
    Lithium naphthalenide presents itself as a mild and efficient reagent for the cleavage of α,β-epoxy ketones to give the corresponding β-hydroxy ketones in good yields.
    萘基锂化合物作为一种温和且高效的试剂,能够有效地切割α,β-环氧酮,从而以良好的产率生成相应的β-羟基酮。
  • Microbial hydroxylation of steroids. Part 12. Hydroxylation of testosterone and related steroids by <i>Gnomonia</i><i>fructicola</i> ATCC 11430
    作者:Herbert L. Holland、Frances M. Brown、P. Chinna Chenchaiah、Michael J. Chernishenko、Shaheer H. Khan、J. Appa Rao
    DOI:10.1139/v89-044
    日期:1989.2.1

    The fungus Gnomoniafructicola ATCC 11430 hydroxylates testosterone at C-2β in 40–60% yield. The enzyme involved has been shown to be an inducible CO sensitive, cyanide insensitive oxygenase, with a requirement for theΔ4-3-ketosteroid substrate functionality. The use of 2α- and 2β-deuterium labelled substrates has shown that hydrogen loss from C-2 during 2β hydroxylation is isotope dependent and non-stereospecific. This is interpreted in terms of a Δ2,4-dienolic enzyme-bound intermediate form of the substrate. Keywords: Gnomoniafructicola, hydroxylation, steroids, testosterone.

    真菌Gnomoniafructicola ATCC 11430以40-60%的产率在C-2β处对睾酮进行羟基化。所涉及的酶已被证明是一种可诱导的CO敏感、氰化物不敏感的氧化酶,需要Δ4-3-酮类固醇底物的功能性。使用2α-和2β-氘标记底物表明,在2β羟基化过程中,C-2处的氢损失是同位素依赖的,且不具有立体特异性。这被解释为底物的Δ2,4-二烯醇酶结合中间体形式。关键词:Gnomoniafructicola、羟基化、类固醇、睾酮。
  • Hydrazine hydrate induced reductive cleavage of α,β-epoxy ketones: an efficient procedure for the preparation of β-hydroxy ketones
    作者:Jorge A.R. Salvador、Alcino J.L. Leitão、M. Luísa Sá e Melo、James R. Hanson
    DOI:10.1016/j.tetlet.2004.12.103
    日期:2005.2
    An efficient and general procedure for the reductive cleavage of α,β-epoxy ketones to the corresponding β-hydroxy ketones, using hydrazine hydrate in ethanol at low temperatures, is described.
    描述了一种在低温下使用水合肼在乙醇中将α,β-环氧酮还原裂解为相应的β-羟基酮的有效且通用的方法。
  • Bell,A.M. et al., Journal of the Chemical Society. Perkin transactions I, 1973, p. 2131 - 2136
    作者:Bell,A.M. et al.
    DOI:——
    日期:——
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