메뉴 건너뛰기




Volumn 45, Issue 33, 2006, Pages 5487-5491

[1,2,3]Triazolo[4,5-b]porphyrins: New building blocks for porphyrinic materials

Author keywords

Alkylation; Arylation; Macrocycles; Nitrogen heterocycles; Porphyrinoids

Indexed keywords

ARYLATION; MACROCYCLES; NITROGEN HETEROCYCLES; PORPHYRINOIDS;

EID: 33748645541     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200600747     Document Type: Article
Times cited : (59)

References (64)
  • 10
    • 0034599933 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1288-1292.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1288-1292
  • 21
    • 0034678577 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1458-1462.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1458-1462
  • 23
    • 0032538774 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 3023-3027.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 3023-3027
  • 28
    • 0034679490 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 2549-2552;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 2549-2552
  • 35
    • 0242355014 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 4966-4970.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4966-4970
  • 45
    • 0000756640 scopus 로고
    • (Eds.: D. H. R. Barton, W. D. Ollis), Pergamon, Oxford
    • M. R. Grimmett in Comprehensive Organic Chemistry, Vol. 4 (Eds.: D. H. R. Barton, W. D. Ollis), Pergamon, Oxford, 1979, p. 357.
    • (1979) Comprehensive Organic Chemistry, Vol. 4 , vol.4 , pp. 357
    • Grimmett, M.R.1
  • 46
    • 84943402961 scopus 로고
    • (Eds.: A. R. Katritzky, C. W. Rees), Pergamon, Oxford
    • H. Wamhoff in Comprehensive Heterocyclic Chemistry, Vol. 5 (Eds.: A. R. Katritzky, C. W. Rees), Pergamon, Oxford, 1984, Part 4A, p. 669.
    • (1984) Comprehensive Heterocyclic Chemistry, Vol. 5 , vol.5 , Issue.PART 4A , pp. 669
    • Wamhoff, H.1
  • 48
    • 33748645842 scopus 로고    scopus 로고
    • note
    • N-Unsubstituted 1,2,3-triazoles exist in two tautomeric forms (1H- and 2H-) that are in equilibrium both in solution and in the gas phase. For simplification, compounds 2 are represented as 2H-triazoles, independently of the predominant tautomer.
  • 49
    • 0003946851 scopus 로고
    • (Ed.: K. M. Smith), Elsevier, Amsterdam
    • "General features of the structure and chemistry of porphyrin compounds" K. M. Smith in Porphyrins and Metalloporphyrins (Ed.: K. M. Smith), Elsevier, Amsterdam, 1975, p. 21.
    • (1975) Porphyrins and Metalloporphyrins , pp. 21
    • Smith, K.M.1
  • 57
    • 3242702077 scopus 로고    scopus 로고
    • Broker AXS Inc., Madison, Wisconsin, USA
    • SAINT+. Version 6.45. Broker AXS Inc., Madison, Wisconsin, USA, 2003.
    • (2003) SAINT+. Version 6.45
  • 64
    • 33748659772 scopus 로고    scopus 로고
    • DeLano Scientific, San Carlos, CA, USA
    • "The PyMOL Molecular Graphics System": W. L. DeLano, DeLano Scientific, San Carlos, CA, USA, 2002. http://www.pymol.org
    • (2002)
    • DeLano, W.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.