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Volumn 41, Issue 10, 2000, Pages 1619-1622

Palladium(II)-catalyzed intramolecular 1,2-oxidation of allenes involving nitrogen nucleophiles

Author keywords

Allenes; Cyclization; Nitrogen heterocycles; Palladium catalysis

Indexed keywords

1,4 BENZOQUINONE; ALLENE DERIVATIVE; LACTAM DERIVATIVE; LITHIUM DERIVATIVE; NITROGEN; PALLADIUM; PYRROLIDINE DERIVATIVE; TOLUENESULFONAMIDE DERIVATIVE;

EID: 0034603478     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02343-6     Document Type: Article
Times cited : (36)

References (34)
  • 4
    • 0003321649 scopus 로고
    • (d) Abel, E. W.; Stone, G. A.; Wilkinson, G., Eds.; Pergamon: New York, (vol. Ed. Hegedus, L. S.)
    • (d) Harrington, P. J. In Comprehensive Organometallic Chemistry II; Abel, E. W.; Stone, G. A.; Wilkinson, G., Eds.; Pergamon: New York, 1995; Vol. 12 (vol. Ed. Hegedus, L. S.), pp. 797-904.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 797-904
    • Harrington, P.J.1
  • 24
    • 0342789105 scopus 로고    scopus 로고
    • 8f to give the N-tosylamides 1, 3, 5, 7, 9 and 11
    • 8f to give the N-tosylamides 1, 3, 5, 7, 9 and 11.
  • 30
    • 0343659336 scopus 로고    scopus 로고
    • Ref 1a, p. 166
    • Ref 1a, p. 166.
  • 33
    • 0343223648 scopus 로고    scopus 로고
    • 3) δ 142.9, 136.6, 133.4, 129.1, 127.2, 124.3, 60.4, 49.3, 32.4, 25.8, 25.2, 21.6, 21.1
    • 3) δ 142.9, 136.6, 133.4, 129.1, 127.2, 124.3, 60.4, 49.3, 32.4, 25.8, 25.2, 21.6, 21.1.
  • 34
    • 0032560834 scopus 로고    scopus 로고
    • Compound 18 was probably formed via a palladium-catalyzed intramolecular hydroamination reaction
    • Compound 18 was probably formed via a palladium-catalyzed intramolecular hydroamination reaction; see: Meguro, M.; Yamamoto, Y. Tetrahedron Lett. 1998, 39, 5421.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5421
    • Meguro, M.1    Yamamoto, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.