메뉴 건너뛰기




Volumn 2, Issue 10, 1996, Pages 1197-1200

Porphyrin synthesis by the "3+1" approach: New applications for an old methodology

Author keywords

Aromaticity; MacDonald condensation; Porphyrinoids; Pyrroledialdehydes; Tripyrranes

Indexed keywords

ACID-CATALYZED CONDENSATION; AROMATICITIES; ELECTRON-DEFICIENT; FUSED AROMATIC RINGS; NEW APPLICATIONS; PORPHYRINOIDS; PYRROLEDIALDEHYDES; TRIPYRRANES;

EID: 0002315830     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.19960021004     Document Type: Article
Times cited : (170)

References (70)
  • 7
    • 3142580582 scopus 로고
    • Tetrahedron 1990, 46, 7599.
    • (1990) Tetrahedron , vol.46 , pp. 7599
  • 23
    • 0006368032 scopus 로고
    • Improved syntheses of symmetrically substituted porphyrins have also been the subject of numerous recent investigations: e.g.
    • Improved syntheses of symmetrically substituted porphyrins have also been the subject of numerous recent investigations: e.g. J. S. Lindsey, I. C. Schreiman, H. C. Hsu, P. C. Kearney, A. M. Marguerettaz, J. Org. Chem. 1987, 52, 827;
    • (1987) J. Org. Chem. , vol.52 , pp. 827
    • Lindsey, J.S.1    Schreiman, I.C.2    Hsu, H.C.3    Kearney, P.C.4    Marguerettaz, A.M.5
  • 34
    • 84891315413 scopus 로고    scopus 로고
    • Book of Abstracts, ORGN 179. This work was supported by the National Science Foundation under Grant No. CHE-9500630 and the Donors of the Petroleum Research Fund, administered by the American Chemical Society
    • 210th National Meeting of the American Chemical Society, Chicago, Illinois, (USA). August 1995 (T. D. Lash, Y. Lin, Book of Abstracts, ORGN 179). This work was supported by the National Science Foundation under Grant No. CHE-9500630 and the Donors of the Petroleum Research Fund, administered by the American Chemical Society.
    • 210th National Meeting of the American Chemical Society, Chicago, Illinois, (USA). August 1995
    • Lash, T.D.1    Lin, Y.2
  • 36
    • 0002380986 scopus 로고    scopus 로고
    • A report on the synthesis of a "mono-hook" porphyrin by the "3 + 1" approach was published recently: These authors noted that the acid-catalyzed condensation of diformyltripyrranes with 3,4-diethylpyrrole failed to give any porphyrin products. As the initial condensation is likely to afford an electron-deficient pyrromethene unit that would be unable to react with a second pyrrole aldehyde moiety, this factor presumably prevents porphyrin formation
    • A report on the synthesis of a "mono-hook" porphyrin by the "3 + 1" approach was published recently: J. L. Sessler, J. W. Genge, A. Urbach, P. Sanson, Synlett 1996, 187. These authors noted that the acid-catalyzed condensation of diformyltripyrranes with 3,4-diethylpyrrole failed to give any porphyrin products. As the initial condensation is likely to afford an electron-deficient pyrromethene unit that would be unable to react with a second pyrrole aldehyde moiety, this factor presumably prevents porphyrin formation.
    • (1996) Synlett , pp. 187
    • Sessler, J.L.1    Genge, J.W.2    Urbach, A.3    Sanson, P.4
  • 46
    • 0001329837 scopus 로고
    • Improved syntheses of pyrrolic intermediates have also facilitated these studies. See
    • Improved syntheses of pyrrolic intermediates have also facilitated these studies. See: J. B. Paine III, D. Dolphin, J. Org. Chem. 1985, 50, 5598;
    • (1985) J. Org. Chem. , vol.50 , pp. 5598
    • Paine III, J.B.1    Dolphin, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.