Robust Organocatalytic Three-Component Approach to 1,3-Diarylallylidene Pyrazolones via Consecutive Double Condensation Reactions

被引:0
|
作者
Patel, Ashvani K. [1 ]
Samanta, Sampak [1 ]
机构
[1] Indian Inst Technol Indore, Dept Chem, Simrol 453552, Madhya Pradesh, India
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 23期
关键词
STEREOSELECTIVE-SYNTHESIS; UNSATURATED PYRAZOLONES; ALLYLIC ALKYLATION; DERIVATIVES; SPIROOXINDOLES; INHIBITORS; CHEMISTRY; OXINDOLES; SEQUENCE; CASCADE;
D O I
10.1021/acs.joc.4c02273
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A robust pyrrolidine-BzOH salt-catalyzed one-pot three-component reaction involving 4-unsubstituted pyrazolones, aryl/heteroarylaldehydes, and aryl methyl ketones is reported for the first time. This catalytic process fortifies an efficient method, allowing for the practical synthesis of a wide array of synthetically useful 1,3-diarylallylidene pyrazolones in good to high yields exclusively in their single geometrical isomer forms. Furthermore, this catalyst facilitates a sequential double condensation reaction under thermal conditions, thereby enabling two consecutive C=C bonds through displacement of aryl groups. Moreover, this organocatalytic technique achieves a 100% carbon atom economy, marking a significant step forward toward efficient and sustainable synthesis.
引用
收藏
页码:17528 / 17543
页数:16
相关论文
共 50 条
  • [1] Organocatalytic Three-Component 1,2-Cyanoalkylacylation of Alkenes via Radical Relay
    Gao, Yu
    Quan, Yusheng
    Li, Zhenjiang
    Gao, Luoyu
    Zhang, Zhihao
    Zou, Xin
    Yan, Rui
    Qu, Yuanyuan
    Guo, Kai
    ORGANIC LETTERS, 2021, 23 (01) : 183 - 189
  • [2] Enantioselective Construction of the Biologically Significant Dibenzo[1,4]diazepine Scaffold via Organocatalytic Asymmetric Three-Component Reactions
    Wang, Yang
    Tu, Man-Su
    Shi, Feng
    Tu, Shu-Jiang
    ADVANCED SYNTHESIS & CATALYSIS, 2014, 356 (09) : 2009 - 2019
  • [3] Asymmetric organocatalytic three-component 1,3-dipolar cycloaddition: Control of stereochemistry via a chiral bronsted acid activated dipole
    Chen, Xiao-Hua
    Zhang, Wen-Quan
    Gong, Liu-Zhu
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (17) : 5652 - +
  • [4] Three-component condensation of 1,3-dimethyl-barbituric acid, arylglyoxals, and substituted thioureas
    Kolos, N. N.
    Zamigailo, L. L.
    Chechina, N. V.
    Omel'chenko, I. V.
    Shishkin, O. V.
    Vashchenko, E. V.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2013, 48 (12) : 1817 - 1823
  • [5] Three-component condensation of 1,3-dimethyl-barbituric acid, arylglyoxals, and substituted thioureas
    N. N. Kolos
    L. L. Zamigailo
    N. V. Chechina
    I. V. Omel’chenko
    O. V. Shishkin
    E. V. Vashchenko
    Chemistry of Heterocyclic Compounds, 2013, 48 : 1817 - 1823
  • [6] A simple and effective approach to the synthesis of rhodanine derivatives via three-component reactions in water
    Alizadeh, Abdolati
    Rostamnia, Sadegh
    Zohreh, Nasrin
    Hosseinpour, Reza
    TETRAHEDRON LETTERS, 2009, 50 (14) : 1533 - 1535
  • [7] Three-component condensation of 6-amino-quinoline with aromatic aldehydes and cyclic 1,3-diketones
    Kozlov, N. G.
    Gusak, K. N.
    Tkachev, A. V.
    KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 2007, (06): : 877 - 885
  • [8] Diastereospecific entry to pyrrolidinyldispirooxindole skeletons via three-component 1,3-dipolar cycloadditions
    Qian, Yu-Lun
    Li, Bo
    Xia, Peng-Ju
    Wang, Jing
    Xiang, Hao-Yue
    Yang, Hua
    TETRAHEDRON, 2018, 74 (47) : 6821 - 6828
  • [9] Facile synthesis of 1,4-diketones via three-component reactions of α-ketoaldehyde, 1,3-dicarbonyl compound, and a nucleophile in water
    Yang, Jian
    Mei, Fuming
    Fu, Shitao
    Gu, Yanlong
    GREEN CHEMISTRY, 2018, 20 (06) : 1367 - 1374
  • [10] Photoinduced three-component reactions of tetracyanobenzene with alkenes in the presence of 1,3-dicarbonyl compounds as nucleophiles
    Lu, Zhi-Feng
    Shen, Yong-Miao
    Yue, Jia-Jun
    Hu, Hong-Wen
    Xu, Jian-Hua
    JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (20): : 8010 - 8015