Electrochemical synthesis of [1,2,4]oxadiazol-3-one derivatives:: anodic oxidation of N-amidoimidates

被引：4
|
作者：
Tapsoba, I [1 ]
Adhoum, N [1 ]
Ben Khoud, ML [1 ]
Boujlel, K [1 ]
机构：
[1] Fac Sci Tunis, Lab Chim Analyt & Electrochim, Tunis 1002, Tunisia
来源：
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 2003年 / 553卷
关键词：
anodic oxidation; n-amidoimidates; oxadiazolone;
D O I：
10.1016/S0022-0728(03)00252-3
中图分类号：
O65 [分析化学];
学科分类号：
070302 ; 081704 ;
摘要：
Anodic oxidation of N-amidoimidates was performed in acetonitrile + lithium perchlorate as the electrolyte solution at platinum using controlled potentials. The products, isolated in good yield after oxidation of the amide group followed by deprotonation and intramolecular cyclization reactions, were identified as [1,2,4]oxadiazol-3-one derivatives. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码：21 / 25
页数：5
相关论文
共 50 条
  • [1] Electrochemical synthesis of 1,2,4-triazol-3-thione derivatives:: Anodic oxidation of N-thioamidohydrazones
    Chmekh, Rania
    Tapsoba, Issa
    Medini, Hayet
    Maisonhaute, Emmanuel
    Benkhoud, Mohamed Lamine
    Boujlel, Khaled
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2007, 599 (01): : 85 - 90
  • [2] NEW SYNTHESIS OF 4,5-DIHYDRO-1,2,4-TRIAZIN-3(2H)-ONE DERIVATIVES THROUGH CYCLIC TRANSFORMATION OF 1,3,4-OXADIAZOL-2(3H)-ONE DERIVATIVES
    MILCENT, R
    YVER, B
    BARBIER, G
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1992, 29 (04) : 959 - 962
  • [3] Synthesis and Anticancer Activity of 1,2,4-Oxadiazol Linked Benzimidazole Derivatives
    Srinivas, M.
    Satyaveni, S.
    Ram, B.
    RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2018, 88 (12) : 2653 - 2657
  • [4] Synthesis and Anticancer Activity of 1,2,4-Oxadiazol Linked Benzimidazole Derivatives
    M. Srinivas
    S. Satyaveni
    B. Ram
    Russian Journal of General Chemistry, 2018, 88 : 2653 - 2657
  • [5] Synthesis of new derivatives of 1,2,4-triazol-3-one
    Struga, M.
    Dobosz, M.
    Kossakowski, J.
    Dybala, I.
    Stepniak, K.
    Koziol, A. E.
    POLISH JOURNAL OF CHEMISTRY, 2006, 80 (06) : 889 - 897
  • [6] A new class of selective myocardial calcium channel modulators. 2. Role of the acetal chain in oxadiazol-3-one derivatives
    Budriesi, R
    Carosati, E
    Chiarini, A
    Cosimelli, B
    Cruciani, G
    Ioan, P
    Spinelli, D
    Spisani, R
    JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (07) : 2445 - 2456
  • [7] Synthesis and antimicrobial activities of 2-(5-mercapto)-1,3-oxadiazol-2-ylmethyl-1,2,4-triazol-3-one derivatives
    Demirbas, Ahmet
    Sahin, Deniz
    Demirbas, Neslihan
    Karaoglu, Senguel Alpay
    Bektas, Hakan
    TURKISH JOURNAL OF CHEMISTRY, 2010, 34 (03) : 347 - 358
  • [8] Molecular mechanics study of the inclusion complexes of some 1,2,4-oxadiazole derivatives of 3,3′-bis (1,2,4-oxadiazol-5(4H)-one) with β-cyclodextrin
    Al-Sou'od, KA
    JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2006, 54 (1-2) : 123 - 127
  • [9] Molecular Mechanics Study of the Inclusion Complexes of Some 1,2,4-Oxadiazole Derivatives of 3,3′-Bis (1,2,4-Oxadiazol-5(4H)-one) with β-Cyclodextrin
    Khaldoun A. Al-Sou’od
    Journal of inclusion phenomena and macrocyclic chemistry, 2006, 54 : 123 - 127
  • [10] One pot synthesis of some new spiro[3H-indol-3,5′(4′H)-[1,2,4] oxadiazol]-2-ones and bis[spiro[3H-indol-3,5′(4′H)-[1,2,4] oxadiazol]-2-ones]
    Azizian, J
    Jadidi, K
    Mehrdad, M
    Sarrafi, Y
    SYNTHETIC COMMUNICATIONS, 2000, 30 (13) : 2309 - 2315
12345