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Volumn 4, Issue 3, 1998, Pages 508-511

Carbachlorins

Author keywords

Aromaticity; Carbaporphyrins; Chlorins; Porphyrinoids; Tripyrranes

Indexed keywords


EID: 0009069893     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(19980310)4:3<508::AID-CHEM508>3.0.CO;2-O     Document Type: Article
Times cited : (63)

References (35)
  • 5
    • 11944260641 scopus 로고
    • S. B. Brown, T. G. Truscott, Chem. Br. 1993, 29, 955; R. Bonnett, Chem. Soc. Rev. 1995, 24, 19.
    • (1995) Chem. Soc. Rev. , vol.24 , pp. 19
    • Bonnett, R.1
  • 6
    • 0003946851 scopus 로고    scopus 로고
    • A. W. Johnson in ref. [3], pp. 729-754; B. Franck, A. Nonn, Angew. Chem. 1995, 107, 1941; Angew. Chem. Int. Ed. Engl. 1995, 34, 1795; E. Vogel, J. Heterocyclic Chem. 1996, 33, 1461; J. Ayub, D. Dolphin, Chem. Rev. 1997, 97, 2267-2340.
    • Porphyrins and Metalloporphyrins , pp. 729-754
    • Johnson, A.W.1
  • 7
    • 0001563101 scopus 로고
    • A. W. Johnson in ref. [3], pp. 729-754; B. Franck, A. Nonn, Angew. Chem. 1995, 107, 1941; Angew. Chem. Int. Ed. Engl. 1995, 34, 1795; E. Vogel, J. Heterocyclic Chem. 1996, 33, 1461; J. Ayub, D. Dolphin, Chem. Rev. 1997, 97, 2267-2340.
    • (1995) Angew. Chem. , vol.107 , pp. 1941
    • Franck, B.1    Nonn, A.2
  • 8
    • 33748216387 scopus 로고
    • A. W. Johnson in ref. [3], pp. 729-754; B. Franck, A. Nonn, Angew. Chem. 1995, 107, 1941; Angew. Chem. Int. Ed. Engl. 1995, 34, 1795; E. Vogel, J. Heterocyclic Chem. 1996, 33, 1461; J. Ayub, D. Dolphin, Chem. Rev. 1997, 97, 2267-2340.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1795
  • 9
    • 0001663911 scopus 로고    scopus 로고
    • A. W. Johnson in ref. [3], pp. 729-754; B. Franck, A. Nonn, Angew. Chem. 1995, 107, 1941; Angew. Chem. Int. Ed. Engl. 1995, 34, 1795; E. Vogel, J. Heterocyclic Chem. 1996, 33, 1461; J. Ayub, D. Dolphin, Chem. Rev. 1997, 97, 2267-2340.
    • (1996) J. Heterocyclic Chem. , vol.33 , pp. 1461
    • Vogel, E.1
  • 10
    • 0001299658 scopus 로고    scopus 로고
    • A. W. Johnson in ref. [3], pp. 729-754; B. Franck, A. Nonn, Angew. Chem. 1995, 107, 1941; Angew. Chem. Int. Ed. Engl. 1995, 34, 1795; E. Vogel, J. Heterocyclic Chem. 1996, 33, 1461; J. Ayub, D. Dolphin, Chem. Rev. 1997, 97, 2267-2340.
    • (1997) Chem. Rev. , vol.97 , pp. 2267-2340
    • Ayub, J.1    Dolphin, D.2
  • 11
    • 0142192484 scopus 로고
    • H. J. Callot, E. Schaeffer, Tetrahedron 1978, 34, 2295; E Vogel, M. Kocher, M. Balchi, I. Teichler, J. Lex, H. Schmickler, O. Ermer, Angew. Chem. 1987, 99, 912; Angew. Chem. Int. Ed. Engl. 1987, 36, 931.
    • (1978) Tetrahedron , vol.34 , pp. 2295
    • Callot, H.J.1    Schaeffer, E.2
  • 13
    • 0142192484 scopus 로고
    • H. J. Callot, E. Schaeffer, Tetrahedron 1978, 34, 2295; E Vogel, M. Kocher, M. Balchi, I. Teichler, J. Lex, H. Schmickler, O. Ermer, Angew. Chem. 1987, 99, 912; Angew. Chem. Int. Ed. Engl. 1987, 36, 931.
    • (1987) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 931
  • 14
    • 0027156784 scopus 로고    scopus 로고
    • For a review on the synthesis of chlorophylls, see K. M. Smith in ref. [1]. pp. 115-143. For syntheses of less-common natural hydroporphyrins, see ref. [2]. Recent chlorin syntheses include : D. H. Burns, T. M. Caldwell, M. W. Burden, Tetrahedron Lett. 1993, 34, 2883: L. Jaquinod, C. Gros, R. G. Khoury, K. M. Smith, Chem. Commun. 1996, 2581.
    • Chlorophylls , pp. 115-143
    • Smith, K.M.1
  • 15
    • 0027156784 scopus 로고    scopus 로고
    • For a review on the synthesis of chlorophylls, see K. M. Smith in ref. [1]. pp. 115-143. For syntheses of less-common natural hydroporphyrins, see ref. [2]. Recent chlorin syntheses include : D. H. Burns, T. M. Caldwell, M. W. Burden, Tetrahedron Lett. 1993, 34, 2883: L. Jaquinod, C. Gros, R. G. Khoury, K. M. Smith, Chem. Commun. 1996, 2581.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 2883
    • Burns, D.H.1    Caldwell, T.M.2    Burden, M.W.3
  • 16
    • 0029804082 scopus 로고    scopus 로고
    • For a review on the synthesis of chlorophylls, see K. M. Smith in ref. [1]. pp. 115-143. For syntheses of less-common natural hydroporphyrins, see ref. [2]. Recent chlorin syntheses include : D. H. Burns, T. M. Caldwell, M. W. Burden, Tetrahedron Lett. 1993, 34, 2883: L. Jaquinod, C. Gros, R. G. Khoury, K. M. Smith, Chem. Commun. 1996, 2581.
    • (1996) Chem. Commun. , pp. 2581
    • Jaquinod, L.1    Gros, C.2    Khoury, R.G.3    Smith, K.M.4
  • 17
    • 0000327747 scopus 로고    scopus 로고
    • T. D. Lash, M. J. Hayes, Angew. Chem. 1997, 109, 868; Angew. Chem. Int. Ed. Engl. 1997, 36, 840.
    • (1997) Angew. Chem. , vol.109 , pp. 868
    • Lash, T.D.1    Hayes, M.J.2
  • 18
    • 0030916482 scopus 로고    scopus 로고
    • T. D. Lash, M. J. Hayes, Angew. Chem. 1997, 109, 868; Angew. Chem. Int. Ed. Engl. 1997, 36, 840.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 840
  • 19
    • 0011246374 scopus 로고    scopus 로고
    • K. Berlin, Angew. Chem. 1996, 108, 1955: Angew. Chem. Int. Ed. Engl. 1996, 35, 1820.
    • (1996) Angew. Chem. , vol.108 , pp. 1955
    • Berlin, K.1
  • 20
    • 0030485295 scopus 로고    scopus 로고
    • K. Berlin, Angew. Chem. 1996, 108, 1955: Angew. Chem. Int. Ed. Engl. 1996, 35, 1820.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1820
  • 21
    • 0002315830 scopus 로고    scopus 로고
    • T. D. Lash, Chem. Eur. J. 1996, 2, 1197. A popularized account of these studies has also appeared in Chem. Eng. News 1997, 75 (35), 31-33.
    • (1996) Chem. Eur. J. , vol.2 , pp. 1197
    • Lash, T.D.1
  • 22
    • 34547982093 scopus 로고    scopus 로고
    • A popularized account of these studies has also appeared
    • T. D. Lash, Chem. Eur. J. 1996, 2, 1197. A popularized account of these studies has also appeared in Chem. Eng. News 1997, 75 (35), 31-33.
    • (1997) Chem. Eng. News , vol.75 , Issue.35 , pp. 31-33
  • 24
    • 0000059175 scopus 로고
    • T. D. Lash, Angew. Chem. 1995, 107, 2703; Angew. Chem. Int. Ed. Engl. 1995, 34, 2533.
    • (1995) Angew. Chem. , vol.107 , pp. 2703
    • Lash, T.D.1
  • 25
    • 33750614446 scopus 로고
    • T. D. Lash, Angew. Chem. 1995, 107, 2703; Angew. Chem. Int. Ed. Engl. 1995, 34, 2533.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 2533
  • 28
  • 29
    • 0030905554 scopus 로고    scopus 로고
    • T. D. Lash, S. T. Chaney, Angew. Chem. 1997, 109, 867; Angew. Chem. Int. Ed. Engl. 1997, 36, 839.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 839
  • 30
    • 34547995917 scopus 로고    scopus 로고
    • M. J. Hayes, T. D. Lash, unpublished results
    • M. J. Hayes, T. D. Lash, unpublished results.
  • 33
    • 34547993501 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy indicates that our samples of 7 consisted primarily of the endo form, but approximately 5% of the exo isomer was also present.
  • 35
    • 34547997463 scopus 로고    scopus 로고
    • note
    • In some cases, moss-green crystals were obtained for carbachlorin 11. These samples were otherwise indistinguishable from the purple crystals that were more commonly observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.