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exo,syn-2-(hydroxy(4-nitrophenyl)methyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-one

中文名称
——
中文别名
——
英文名称
exo,syn-2-(hydroxy(4-nitrophenyl)methyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-one
英文别名
(1R,2S,5S)-2-[(S)-hydroxy-(4-nitrophenyl)methyl]-8-methyl-8-azabicyclo[3.2.1]octan-3-one
exo,syn-2-(hydroxy(4-nitrophenyl)methyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-one化学式
CAS
——
化学式
C15H18N2O4
mdl
——
分子量
290.319
InChiKey
FNCVBADSOYVOML-CTHBEMJXSA-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):
    1.6
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    86.4
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

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文献信息

  • Environmentally benign diastereoselective synthesis of granatane and tropane aldol derivatives
    作者:Aneta Nodzewska、Agnieszka Bokina、Katarzyna Romanowska、Ryszard Lazny
    DOI:10.1039/c4ra02834a
    日期:——
    Direct aldol reactions of tropinone and granatanone (pseudopelletierine) with aromatic aldehydes were promoted by the presence of water. The anti–syn-diastereoselectivity depended on the amount of water used or on the possibility of product precipitation from the reaction mixture. Some of the reactions showed excellent atom economy, a low E factor, and high diastereoselectivity (up to 98%). In several cases ‘seeding’ with the anti isomer, used to induce the deposition of solid products, improved the conversion (up to 1.8 times) and the anti–syn ratio (up to 98 : 2). The applicability of spontaneous direct aldol reactions in the presence of water was also extended to N-alkyl nortropanones or norgranatanones using an aqueous–organic medium. However, under these conditions only the exo,syn isomers of the N-substituted aldols were obtained. The syn-selectivity for the tropane- and granatane-related aldols is specific for water-promoted reactions and results from thermodynamic control.
    的存在促进了托品酮和石榴酮(伪派尔特利林)与芳香醛的直接 aldol 反应。反应的反对–顺代谢选择性取决于使用的的量或反应混合物中产物沉淀的可能性。一些反应表现出优异的原子经济性、较低的 E 因素和高达 98% 的立体选择性。在几个案例中,使用反对异构体进行“引种”,以诱导固体产物的沉淀,提高了转化率(高达 1.8 倍)和反对–顺比(高达 98:2)。在的存在下,自发直接 aldol 反应的适用性也扩展到了 N-烷基北托品酮或北石榴酮,采用-有机介质。然而,在这些条件下,只获得了 N-取代的 aldol 的外,顺异构体。对于与托品和石榴相关的 aldol,顺选择性是促进反应所特有的,源于热力学控制。
  • A DFT study of the origins of the stereoselectivity in the aldol reaction of bicyclic amino ketones in the presence of water
    作者:Ryszard Lazny、Artur Ratkiewicz、Aneta Nodzewska、Joanna Wysocka
    DOI:10.1016/j.tetlet.2012.08.070
    日期:2012.10
    anti/syn-diastereomeric ratio (dr) for the solvent-less reaction of tropinone with several aromatic aldehydes. The CPCM-B3LYP/6-31g(d) method reproduces the anti/syn-diastereomeric ratio of the aqueous aldol reaction of tropinone with several aromatic aldehydes with reasonable deviation (0–88%), excellent (0–10)% agreement was found for the reactions of tropinone and granatanone with benzaldehyde. Qualitatively
    蛋白(8-甲基-8-氮杂双环[3.2.1] octan-3-one)和格拉纳酮(伪松油碱,9-甲基-9-氮杂双环[3.3.1]的直接无溶剂(纯)羟醛反应的实验非对映选择性。 ] nonan-3-one)在催化量的的存在下,最精确地通过理论上B3LYP / 6-31g(d)的气相计算的异构体的热力学分布来精确再现。小于30%的系统误差,平均而言,存在于所预测的反/顺式-diastereomeric比(博士为托品酮的与几个芳族醛的无溶剂型反应)。CPCM-B3LYP / 6-31g(d)方法复制了anti / syn-肌蛋白与几种芳香族醛性羟醛反应的非对映体比率(合理偏差(0–88%),极好(0-10)%)被认为是肌蛋白和格拉纳坦酮与苯甲醛的反应。还发现在不同溶剂(DMF,THF和Et 3 N)中的dr值在质量上令人满意。密度泛函理论(DFT)的结果支持了反应热力学控制的概念。
  • Spontaneous and diastereoselective aldol reactions of cyclic β-amino ketones in the presence of water
    作者:Ryszard Lazny、Aneta Nodzewska、Iwona Tomczuk
    DOI:10.1016/j.tetlet.2011.08.107
    日期:2011.10
    Direct aldol reactions of 4-methyl-1-piperidone, tropinone and granatanone (pseudopelletierine) take place spontaneously in the presence of water without any catalyst or additional reagents. The anti/syn-diastereoselectivity of the aqueous aldol reaction depends on the amount of water used. The syn-selectivity of the reaction is probably due to the thermodynamic control. Excellent atom economy and low E factors together with anti-selectivity as high as 98:2 for the tropinone aldol were obtained. (C) 2011 Elsevier Ltd. All rights reserved.
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