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Volumn 51, Issue 49, 2012, Pages 12357-12361

Preferential formation of cyclic trimers by palladium-catalyzed oxidative coupling reactions of 2,18-diethynylporphyrins

Author keywords

alkyne coupling; butadiyne bridge; palladium; porphyrinoids; triporphyrin synthesis

Indexed keywords

ALKYNE COUPLING; BUTADIYNE; CYCLIC DIMERS; CYCLIC TRIMERS; HEXAMERS; OXIDATIVE COUPLING REACTIONS; OXIDATIVE COUPLINGS; PALLADIUM-CATALYZED; PORPHYRINOIDS;

EID: 84870548213     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201207763     Document Type: Article
Times cited : (23)

References (54)
  • 7
    • 78651396127 scopus 로고    scopus 로고
    • (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), World Scientific Publishing, Singapore
    • N. Aratani, A. Osuka, in Handbook of Porphyrin Science, Vol. 1 (Eds.:, K. M. Kadish, K. M. Smith, R. Guilard,), World Scientific Publishing, Singapore, 2010, pp. 1.
    • (2010) Handbook of Porphyrin Science, Vol. 1 , pp. 1
    • Aratani, N.1    Osuka, A.2
  • 40
    • 67849110063 scopus 로고    scopus 로고
    • the case of dibenz[a,j]anthracene-based macrocycle formations, dimers were the main products
    • In the case of dibenz[a,j]anthracene-based macrocycle formations, dimers were the main products;, J. M. W. Chan, J. R. Tischler, S. E. Kooi, V. Bulovic, T. M. Swager, J. Am. Chem. Soc. 2009, 131, 5659.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 5659
    • Chan, J.M.W.1    Tischler, J.R.2    Kooi, S.E.3    Bulovic, V.4    Swager, T.M.5
  • 41
    • 84870478977 scopus 로고    scopus 로고
    • w=0.2443 (all data), GOF=1.037 (I>2.0Ï(I)). CCDC 899883 (3 Ni), 899882 (2 Ni) and 899881 (1 Ni) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 51
    • 84857978292 scopus 로고    scopus 로고
    • For ring-closure processes, Pd-catalyzed acetylene coupling reactions were sometimes adopted. See Refs [3, 5] and a recent review
    • For ring-closure processes, Pd-catalyzed acetylene coupling reactions were sometimes adopted. See Refs [3, 5] and a recent review;, M. Iyoda, J. Yamakawa, M. J. Rahman, Angew. Chem. 2011, 123, 10708
    • (2011) Angew. Chem. , vol.123 , pp. 10708
    • Iyoda, M.1    Yamakawa, J.2    Rahman, M.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.