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Volumn 53, Issue 10, 2014, Pages 2611-2614

Direct meso-alkynylation of metalloporphyrins through gold catalysis for hemoprotein engineering

Author keywords

chemical biology; click chemistry; H NOX proteins; heme proteins; transition metal catalysis

Indexed keywords

CHEMICAL BIOLOGY; CLICK CHEMISTRY; COPPER CATALYZED AZIDE ALKYNE CYCLOADDITION; COPPER(I) CATALYZED AZIDE ALKYNE CYCLOADDITION (CUAAC); HEME PROTEINS; HYPERVALENT IODINE REAGENTS; METALLO-PORPHYRINS; TRANSITION METAL CATALYSIS;

EID: 84897653116     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201310145     Document Type: Article
Times cited : (25)

References (46)
  • 4
    • 60749134505 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1550-1574
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1550-1574
  • 6
    • 77956792503 scopus 로고    scopus 로고
    • (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), World Scientific Publishing Co. Pte. Ltd. Singapore
    • T. Hayashi, in Handbook of Porphyrin Science Vol. 5 (Eds.:, K. M. Kadish, K. M. Smith, R. Guilard,), World Scientific Publishing Co. Pte. Ltd., Singapore, 2010, pp. 1-69
    • (2010) Handbook of Porphyrin Science , vol.5 , pp. 1-69
    • Hayashi, T.1
  • 9
    • 84875850730 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 4088-4106.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 4088-4106
  • 18
    • 84882995566 scopus 로고    scopus 로고
    • (Eds.: I. R. Phillips, E. A. Shephard, P. R. Montellano), Springer Science+Business Media, New York
    • M. B. Winter, J. J. Woodward, M. A. Marletta, in Methods Mol. Biol., Vol. 987 (Eds.:, I. R. Phillips, E. A. Shephard, P. R. Montellano,), Springer Science+Business Media, New York, 2013, pp. 95-106.
    • (2013) Methods Mol. Biol. , vol.987 , pp. 95-106
    • Winter, M.B.1    Woodward, J.J.2    Marletta, M.A.3
  • 22
    • 84879882396 scopus 로고    scopus 로고
    • H. Yorimitsu, A. Osuka, Asian J. Org. Chem. 2013, 2, 356-373; For a broader overview of the meso derivatization of porphyrins, see the Supporting Information.
    • (2013) Asian J. Org. Chem. , vol.2 , pp. 356-373
    • Yorimitsu, H.1    Osuka, A.2
  • 24
    • 33845546747 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 7896-7936
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7896-7936
  • 28
    • 72949089743 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9346-9349.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9346-9349
  • 30
    • 77957334631 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 7304-7307
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 7304-7307
  • 32
    • 84879391123 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 6743-6747.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 6743-6747
  • 35
    • 0017794463 scopus 로고
    • (Eds.: S. Fleischer, L. Packer), Academic Press, New York
    • M. L. Smith, W. S. Caughey, in Methods Enzymology, Vol. 52 (Eds.:, S. Fleischer, L. Packer,), Academic Press, New York, 1978, pp. 421-436.
    • (1978) Methods Enzymology , vol.52 , pp. 421-436
    • Smith, M.L.1    Caughey, W.S.2
  • 36
    • 33846134742 scopus 로고    scopus 로고
    • Y. Q. Zhu, R. B. Silverman, J. Org. Chem. 2007, 72, 233-239. It should be noted that the conclusion in this study was based on the deuteration reaction of a porphyrin in which the vinyl substituents were replaced by ethyl groups. Protoporphyrin IX decomposes at high concentrations of strong deuterated acids.
    • (2007) J. Org. Chem. , vol.72 , pp. 233-239
    • Zhu, Y.Q.1    Silverman, R.B.2
  • 38
    • 72449154666 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9879-9883.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9879-9883
  • 41
    • 84861912742 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 5852-5856
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5852-5856


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.