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Information Journal Paper

Title

THE REGIOSELECTIVE SYNTHESIS OF BROMOCHLORINS RELATED TO CHLOROPHYLL-A FROM METHYL PHEOPHORBIDE-A

Pages

  1139-1145

Keywords

PHOTODYNAMIC THERAPY (PDT) 

Abstract

 An efficient methodology has been developed for the REGIOSELECTIVE SYNTHESIS of brominated CHLORINs related to chlorophyll-a from methyl pheophorbide-a. Several regioselective BROMINATION reactions were accomplished by some particular reaction conditions and a series of conversion of functional group from methyl pheophorbide-a to synthesize mono-, bis- and tri-brominated CHLORINes. The possible mechanisms for the debromination were tentatively proposed and the structures of all new CHLORINs were characterized by elemental analysis, IR, UV-Vis and 1H NMR spectra.

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    • Cite

    APA: Copy

    WANG, J.J., LI, J.Z., & LI, F.G.. (2011). THE REGIOSELECTIVE SYNTHESIS OF BROMOCHLORINS RELATED TO CHLOROPHYLL-A FROM METHYL PHEOPHORBIDE-A. JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS), 8(4), 1139-1145. SID. https://sid.ir/paper/282615/en

    Vancouver: Copy

    WANG J.J., LI J.Z., LI F.G.. THE REGIOSELECTIVE SYNTHESIS OF BROMOCHLORINS RELATED TO CHLOROPHYLL-A FROM METHYL PHEOPHORBIDE-A. JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS)[Internet]. 2011;8(4):1139-1145. Available from: https://sid.ir/paper/282615/en

    IEEE: Copy

    J.J. WANG, J.Z. LI, and F.G. LI, “THE REGIOSELECTIVE SYNTHESIS OF BROMOCHLORINS RELATED TO CHLOROPHYLL-A FROM METHYL PHEOPHORBIDE-A,” JOURNAL OF THE IRANIAN CHEMICAL SOCIETY(JICS), vol. 8, no. 4, pp. 1139–1145, 2011, [Online]. Available: https://sid.ir/paper/282615/en

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