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(3R,5S,1'R)-3-(t-butyldimethylsilyloxy)-5-hydroxy-5-(1'-phenylethoxy) pentanoic acid lactone | 459870-98-5

中文名称
——
中文别名
——
英文名称
(3R,5S,1'R)-3-(t-butyldimethylsilyloxy)-5-hydroxy-5-(1'-phenylethoxy) pentanoic acid lactone
英文别名
(4R,6S)-4-((tert-butyldimethylsilyl)oxy)-6-((R)-1-phenylethoxy)tetrahydro-2H-pyran-2-one;(4R,6S)-4-[tert-butyl(dimethyl)silyl]oxy-6-[(1R)-1-phenylethoxy]oxan-2-one
(3R,5S,1'R)-3-(t-butyldimethylsilyloxy)-5-hydroxy-5-(1'-phenylethoxy) pentanoic acid lactone化学式
CAS
459870-98-5
化学式
C19H30O4Si
mdl
——
分子量
350.53
InChiKey
HFFIVTZEEUMNGX-HFTRVMKXSA-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

物化性质

  • 沸点:
    421.9±45.0 °C(Predicted)
  • 密度:
    1.03±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.82
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Diastereoselective and enantioselective preparation of nor-mevaldic acid surrogates through desymmetrisation methodology. Enantioselective synthesis of (+) and (−) nor-mevalonic lactones
    作者:José Manuel Botubol-Ares、María Jesús Durán-Peña、Rosario Hernández-Galán、Isidro G. Collado、Laurence M. Harwood、Antonio J. Macías-Sánchez
    DOI:10.1016/j.tet.2015.08.010
    日期:2015.10
    Solvent-free desymmetrisation of a meso-dialdehyde with chiral alcohols, led to preparation of 4-silyloxy-6-alkyloxytetrahydro-2H-pyran-2-one derivatives with a 96% de. This methodology, which yields the corresponding methyl nor-mevaldates with 99% ee, has been applied to the enantioselective synthesis of the (−)-(R) and (+)-(S) nor-mevalonic acid lactones.
    的无溶剂的去对称内消旋-dialdehyde与手性醇,导致制备的4-甲硅烷氧基-6- alkyloxytetrahydro -2- ħ -吡喃-2-酮用96%去衍生物。该方法可产生具有99%ee的相应甲基正甲羟戊酸酯,已应用于(-)-(R)和(+)-(S)甲羟戊酸内酯的对映选择性合成。
  • nor-Mevaldic acid surrogates as selective antifungal agent leads against Botrytis cinerea. Enantioselective preparation of 4-hydroxy-6-(1-phenylethoxy)tetrahydro-2H-pyran-2-one
    作者:José Manuel Botubol-Ares、María Jesús Durán-Peña、Rosario Hernández-Galán、Isidro G. Collado、Laurence M. Harwood、Antonio J. Macías-Sánchez
    DOI:10.1016/j.bmc.2015.04.048
    日期:2015.7
    Solvent-free desymmetrisation of meso-dialdehyde 1 with chiral 1-phenylethan-1-ol, led to preparation of 4-silyloxy-6-alkyloxytetrahydro-2H-pyran-2-one (+)-3a with a 96: 4 dr Deprotected lactone (+)-19a and the related racemic lactones 16a-18a present a lactone moiety resembling the natural substrate of HMG-CoA reductase and their antifungal properties have been evaluated against the phytopathogenic fungi Botrytis cinerea and Colletotrichum gloeosporioides. These compounds were selectively active against B. cinerea, while inactive against C. gloeosporioides. (C) 2015 Elsevier Ltd. All rights reserved.
  • Desymmetrisation of dialdehydes: (+)-(S) and (−)-(R) nor-methyl mevaldate as versatile synthetic intermediates
    作者:Shirley L.J. Buckley、Michael G.B. Drew、Laurence M. Harwood、Antonio J. Macı́as-Sánchez
    DOI:10.1016/s0040-4039(02)00533-6
    日期:2002.5
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