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Volumn 46, Issue 1, 2007, Pages 216-220

Synthesis of novel 1, 2, 4-oxadiazole heterocyclic compounds containing 2-H pyranopyridine-2-one moiety and related compounds

Author keywords

1,2,4 oxadiazole; 2H pyranopyridine 2 one; Anti hypertensive; Carboxamide; Carboxamidoxime; Cyclocondensation; Hydroxyl amine; Tyrosine kinase

Indexed keywords


EID: 34548313826     PISSN: 03764699     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (32)
  • 1
    • 84943404144 scopus 로고
    • edited by A R Katritzky & C W Rees, Pergamom Press, and references cited therein
    • Clapp L B, in Comprehensive Heterocyclic Chemistry, edited by A R Katritzky & C W Rees, (Pergamom Press), 6, 1984, p 365 and references cited therein.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.6 , pp. 365
    • Clapp, L.B.1
  • 3
    • 34548300409 scopus 로고    scopus 로고
    • Lima A A, M A Thesis, Departamento de Quimica Fundamental- Universidade Federal de Pernambuco, Recife, 1994.
    • Lima A A, M A Thesis, Departamento de Quimica Fundamental- Universidade Federal de Pernambuco, Recife, 1994.
  • 4
    • 34548364558 scopus 로고    scopus 로고
    • Diana G D & Nitz T J, U S Pat. 5,464,848 (C1. 514-364; C07D413/12), 7 Nov 1995;
    • Diana G D & Nitz T J, U S Pat. 5,464,848 (C1. 514-364; C07D413/12), 7 Nov 1995;
  • 5
    • 34548320051 scopus 로고
    • 869, 287, 15 Apr, 34 pp;
    • US Appl. 869, 287, 15 Apr 1992, 34 pp;
    • (1992) US Appl
  • 6
    • 34548302421 scopus 로고    scopus 로고
    • Chem Abstr, 124, 1996, 124,176114h.
    • Chem Abstr, 124, 1996, 124,176114h.
  • 8
    • 34548359749 scopus 로고
    • 242, 752, 13 May, 74 pp;
    • US appl 242, 752, 13 May 1994, 74 pp;
    • (1994) US appl
  • 9
    • 4243214970 scopus 로고    scopus 로고
    • Chem Abstr 124, 1996, 232462j.
    • (1996) Chem Abstr , vol.124
  • 11
    • 25044467640 scopus 로고
    • Chem Abstr 123, 1995, 340135t.
    • (1995) Chem Abstr , vol.123
  • 13
    • 4243206249 scopus 로고
    • Chem Abstr 123, 1995, 340136u.
    • (1995) Chem Abstr , vol.123
  • 17
    • 15444354604 scopus 로고    scopus 로고
    • Messer Jr W S, Abuh Y F, Liu Y, Periysamy, Nagur D O, Edgar M A A, Ei-Assadi A A, Sbeih S, Dumbar P G, Roknich S, Ryo T, Fang Z, Ojo B, Zhang H, Huzl III J J & Nagy P I, J Med Chem, 40, 1997, 1230;
    • b) Messer Jr W S, Abuh Y F, Liu Y, Periysamy, Nagur D O, Edgar M A A, Ei-Assadi A A, Sbeih S, Dumbar P G, Roknich S, Ryo T, Fang Z, Ojo B, Zhang H, Huzl III J J & Nagy P I, J Med Chem, 40, 1997, 1230;
  • 25
    • 0033575665 scopus 로고    scopus 로고
    • Buchanan J L, Vu C B, Merry T J, Corpuz E G, Pradeepan S G, Main U N, Yang M, Plake H R, Varkhedkar V M, Lynch B A, Loiacono , Tiong C L & Holt D A, Bioorg Med Chem Lett, 9, 1999, 2359;
    • a) Buchanan J L, Vu C B, Merry T J, Corpuz E G, Pradeepan S G, Main U N, Yang M, Plake H R, Varkhedkar V M, Lynch B A, Loiacono , Tiong C L & Holt D A, Bioorg Med Chem Lett, 9, 1999, 2359;
  • 32
    • 34548305623 scopus 로고    scopus 로고
    • Hydroxylamine was prepared from 6.62 g of hydroxylamine hydrochloride and an ethanolic solution of sodium ethoxide 13.2 g stirred for 15 min and filtered the NaCl, the ethanolic solution of hydroxylamine used as such.
    • Hydroxylamine was prepared from 6.62 g of hydroxylamine hydrochloride and an ethanolic solution of sodium ethoxide 13.2 g stirred for 15 min and filtered the NaCl, the ethanolic solution of hydroxylamine used as such.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.