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Volumn 3, Issue 16, 2001, Pages 2501-2504

Preparation of 2,5-disubstituted oxazoles from N-propargylamides

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; DRUG DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; OXAZOLE DERIVATIVE; PALLADIUM; PARGYLINE; SOLVENT;

EID: 0035833708     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016133m     Document Type: Article
Times cited : (148)

References (41)
  • 2
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    • Turchi, I. J., Ed.; Wiley & Sons: New York, Chapter 5
    • (b) Maryanoff, C. A. In Heterocyclic Compounds; Turchi, I. J., Ed.; Wiley & Sons: New York, 1986; Vol. 45, Chapter 5.
    • (1986) Heterocyclic Compounds , vol.45
    • Maryanoff, C.A.1
  • 9
    • 85013550214 scopus 로고
    • Suschitzky, H., Scriven, E. F. V., Eds.; Pergamon Press: Oxford
    • (c) Padwa, A. In Progress in Heterocyclic Chemistry; Suschitzky, H., Scriven, E. F. V., Eds.; Pergamon Press: Oxford, 1994; Vol. 6, pp 56-73.
    • (1994) Progress in Heterocyclic Chemistry , vol.6 , pp. 56-73
    • Padwa, A.1
  • 13
    • 0008167576 scopus 로고
    • Turchi, I. J., Ed.; Wiley & Sons: New York, Chapter 1
    • (d) Turchi, I. J. In Heterocyclic Compounds; Turchi, I. J., Ed.; Wiley & Sons: New York, 1986; Vol. 45, Chapter 1.
    • (1986) Heterocyclic Compounds , vol.45
    • Turchi, I.J.1
  • 21
    • 0042677746 scopus 로고    scopus 로고
    • Gribble G. W., Gilchrist T. L., Eds.; Pergamon Press: Oxford
    • (l) Moody, C. J.; Doyle, K. J. In Progress in Heterocyclic Chemistry; Gribble G. W., Gilchrist T. L., Eds.; Pergamon Press: Oxford, 1997; Vol. 9, pp 1-16.
    • (1997) Progress in Heterocyclic Chemistry , vol.9 , pp. 1-16
    • Moody, C.J.1    Doyle, K.J.2
  • 28
    • 0001848413 scopus 로고    scopus 로고
    • Cacchi, S. J. Organomet. Chem. 1999, 576, 42-64. Cacchi, S. In Perspectives in Organopalladium Chemistry for the XXI Century; Tsuji, J., Ed.; Elsevier: New York 1999; pp 42-64.
    • (1999) Organomet. Chem. , vol.576 , pp. 42-64
    • Cacchi, S.J.1
  • 40
    • 0000037321 scopus 로고    scopus 로고
    • The tendency of tccp to favor the formation of coupling products has been already observed in the palladium-catalyzed reaction of o-ethynyltrifluoroacetanilide with aryl iodides: Cacchi, S.; Fabrizi, G.; Marinelli, F.; Moro, L.; Pace, P. Synlett 1997, 1363-1366.
    • (1997) Synlett , pp. 1363-1366
    • Cacchi, S.1    Fabrizi, G.2    Marinelli, F.3    Moro, L.4    Pace, P.5
  • 41
    • 0042677745 scopus 로고    scopus 로고
    • note
    • 15NO: C, 81.90; H, 6.06; N, 5.62. Found: C, 81.81; H, 6.05; N, 5.64.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.