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Volumn 65, Issue 9, 2000, Pages 2773-2777

Palladium-catalyzed cyclocarbonylation of o-iodoanilines with heterocumulenes: Regioselective preparation of 4(3H)-quinazolinone derivatives

Author keywords

[No Author keywords available]

Indexed keywords

4(3H) QUINAZOLINONE DERIVATIVE; ANILINE DERIVATIVE; CYANAMIDE; ISOCYANIC ACID DERIVATIVE; PALLADIUM; PHOSPHINE; QUINAZOLINE DERIVATIVE;

EID: 0034607706     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo991922r     Document Type: Article
Times cited : (160)

References (62)
  • 1
    • 0008317647 scopus 로고
    • Brown, D. J., Ed.; John Wiley & Sons, Ltd: London
    • (a) Armarego, W. L. F. Quinazolines; Brown, D. J., Ed.; John Wiley & Sons, Ltd: London, 1967.
    • (1967) Quinazolines
    • Armarego, W.L.F.1
  • 51
    • 0000852033 scopus 로고
    • As reported in ref 24, using 2 mol equiv of isocyanate in the reaction with 1 mol of o-iodophenol gave better product yields than performing the reaction using a 1:1 ratio, possibly because dimerization or trimerization of the isocyanate may occur in the presence of base. See: (a) Hofmann, A. W. Ber 1860, 3, 761. Snape, H. L. J. Chem. Soc. 1886, 49, 254. (b) Hofmann, A. W. Ber 1885, 18, 764.
    • (1860) Ber , vol.3 , pp. 761
    • Hofmann, A.W.1
  • 52
    • 0342745244 scopus 로고
    • As reported in ref 24, using 2 mol equiv of isocyanate in the reaction with 1 mol of o-iodophenol gave better product yields than performing the reaction using a 1:1 ratio, possibly because dimerization or trimerization of the isocyanate may occur in the presence of base. See: (a) Hofmann, A. W. Ber 1860, 3, 761. Snape, H. L. J. Chem. Soc. 1886, 49, 254. (b) Hofmann, A. W. Ber 1885, 18, 764.
    • (1886) J. Chem. Soc. , vol.49 , pp. 254
    • Snape, H.L.1
  • 53
    • 0012881339 scopus 로고
    • As reported in ref 24, using 2 mol equiv of isocyanate in the reaction with 1 mol of o-iodophenol gave better product yields than performing the reaction using a 1:1 ratio, possibly because dimerization or trimerization of the isocyanate may occur in the presence of base. See: (a) Hofmann, A. W. Ber 1860, 3, 761. Snape, H. L. J. Chem. Soc. 1886, 49, 254. (b) Hofmann, A. W. Ber 1885, 18, 764.
    • (1885) Ber , vol.18 , pp. 764
    • Hofmann, A.W.1
  • 55
    • 0013282367 scopus 로고
    • Blatt, A. H., Ed.; John Wiley & Sons: New York, Collect
    • Brewster, R. Q. In Organic Syntheses; Blatt, A. H., Ed.; John Wiley & Sons: New York, 1943; Collect. Vol. II, p 347.
    • (1943) Organic Syntheses , vol.2 , pp. 347
    • Brewster, R.Q.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.