Synthesis of pyrazolines via 1,3-dipolar cycloaddition reactions

被引:3
|
作者
Singh, Himanshu [1 ]
Kumar, Rajnish [1 ]
Mazumder, Avijit [1 ]
机构
[1] Noida Inst Engn & Technol, Pharm Inst, Dept Pharmaceut Chem, Greater Noida, India
关键词
1; 3-dipolar cycloaddition; Huisgen zwitter ion; nitrile imines; pyrazolines; synthetic protocols; STEREOSELECTIVE-SYNTHESIS; REGIOSELECTIVE SYNTHESIS; ANTIMICROBIAL ACTIVITIES; BIS-HETEROCYCLES; DERIVATIVES; DIAZOACETATES; DESIGN;
D O I
10.1080/00397911.2023.2201455
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Among the large number of reports published on strategies applicable to the synthesis of pyrazolines and its analogs, The 1,3-dipolar cycloaddition offers a remarkably wide range of utility. Many 1,3-dipolar cycloaddition reactions used for the synthesis of pyrazolines provide better selectivity, eco-friendly, and less expensive chemical processes. In the presented study, we have reviewed various recently adopted strategies for the synthesis of pyrazoline which followed the 1,3-dipolar cycloaddition reactions mechanism and classified them based on starting materials.
引用
收藏
页码:755 / 770
页数:16
相关论文
共 50 条
  • [31] Synthesis of isoxazole conjugates of sugars via 1,3-dipolar cycloaddition
    Vaidya, Vipraja V.
    Wankhede, Karuna S.
    Salunkhe, Manikrao M.
    Trivedi, Girish K.
    CANADIAN JOURNAL OF CHEMISTRY, 2008, 86 (02) : 138 - 141
  • [32] Synthesis of spiro-1-pyrazolines by the 1,3-dipolar cycloaddition of exocyclic α,β-unsaturated ketones with diazomethane
    Lévai, A
    Silva, AMS
    Patonay, T
    Cavaleiro, JAS
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1999, 36 (05) : 1215 - 1222
  • [33] 1,3-DIPOLAR CYCLOADDITION REACTIONS OF ISOCYANATES AND ISOTHIOCYANATES
    VANLOOCK, E
    INDUSTRIE CHIMIQUE BELGE-BELGISCHE CHEMISCHE INDUSTRIE, 1974, 38 (7-8): : 661 - 686
  • [34] 1,3-DIPOLAR CYCLOADDITION REACTIONS OF A HETEROCYCLIC NITRONE
    ALI, SA
    ALMUALLEM, HA
    TETRAHEDRON, 1992, 48 (25) : 5273 - 5282
  • [35] Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions
    Molchanov, A. P.
    Efremova, M. M.
    Kuznetsov, M. A.
    RUSSIAN CHEMICAL BULLETIN, 2022, 71 (04) : 620 - 650
  • [36] Hydrophobic effect on 1,3-dipolar cycloaddition reactions
    Pandey, PS
    Pandey, IK
    TETRAHEDRON LETTERS, 1997, 38 (41) : 7237 - 7240
  • [37] Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review)
    Pronina, Yu. A.
    Teglyai, L. A.
    Ponyaev, A. I.
    Petrov, M. L.
    Boitsov, V. M.
    Stepakov, A. V.
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2024, 94 (01) : 1 - 44
  • [38] Stereoselective synthesis of PEGylated azoles via 1,3-dipolar cycloaddition
    Kazakova, Angelina, V
    Rubicheva, Lyubov G.
    Konev, Alexander S.
    Khlebnikov, Alexander F.
    TETRAHEDRON, 2021, 77
  • [39] Synthesis of functionalized organotrifluoroborates via the 1,3-dipolar cycloaddition of azides
    Molander, Gary A.
    Ham, Jungyeob
    ORGANIC LETTERS, 2006, 8 (13) : 2767 - 2770
  • [40] REACTIONS OF 1,3-DIPOLAR CYCLOADDITION WITH PARTICIPATION OF ALLYLDIPHENYLPHOSPHINE
    STEPANOV, IA
    ZAKHAROV, VI
    CHISTOKLETOV, VN
    PETROV, AA
    ZHURNAL OBSHCHEI KHIMII, 1976, 46 (11): : 2463 - 2467