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Volumn 44, Issue 32, 2005, Pages 5103-5106

Palladium-catalyzed tandem cyclization of bromoenynes through aromatic C-H bond functionalization

Author keywords

C H activation; Cyclization; Enynes; Heterocycles; Palladium

Indexed keywords

CESIUM COMPOUNDS; CHEMICAL BONDS; PALLADIUM;

EID: 23944434406     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200500159     Document Type: Article
Times cited : (61)

References (57)
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    • for a review on organopalladium(IV) chemistry, see: d) A. J. Canty, Acc. Chem. Res. 1992, 25, 83-90.
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    • Canty, A.J.1
  • 21
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    • Angew. Chem. Int. Ed. 2002, 41, 1569-1572;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1569-1572
  • 34
    • 0000704113 scopus 로고
    • b) G. Dyker, Angew. Chem. 1992, 104, 1079-1081;
    • (1992) Angew. Chem. , vol.104 , pp. 1079-1081
    • Dyker, G.1
  • 48
    • 0038451472 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2647-2650;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2647-2650
  • 56
    • 0037420989 scopus 로고    scopus 로고
    • Cesium carbonate in EtOH is a good combination for a cascade palladium-catalyzed cyclization-Suzuki coupling reaction of 2-bromo-1,6-enynes, see: C. H. Oh, Y. M. Lim, Tetrahedron Lett. 2003, 44, 267-270.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 267-270
    • Oh, C.H.1    Lim, Y.M.2
  • 57
    • 33645411471 scopus 로고    scopus 로고
    • note
    • The reaction in EtOH led to cleavage of the tosyl group on the nitrogen atom without formation of the desired tetracyclic product 9h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.