Citation: Jiang Qiyong, Zhang Zhu, Liu Yang, Yao Nannan, Wang Jinjun. Synthesis of Chlorin Aldehydes with Chlorophyllous Skeleton and Their Interactions with Protein[J]. Chinese Journal of Organic Chemistry, ;2017, 37(7): 1814-1823. doi: 10.6023/cjoc201610045 shu

Synthesis of Chlorin Aldehydes with Chlorophyllous Skeleton and Their Interactions with Protein

  • Corresponding author: Wang Jinjun, wjj1955@163.com
  • Received Date: 31 October 2016
    Revised Date: 16 January 2017
    Available Online: 1 July 2017

    Fund Project: the National Natural Science Foundations of China 21272048the University Science and Technology Plan Projects of Shandong Province J15LC51Project supported by the National Natural Science Foundations of China (No. 21272048) and the University Science and Technology Plan Projects of Shandong Province (No. J15LC51)

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  • Pyropheophorbide-a (b) methyl esters were used as starting materials to form different chlorophyll degradation products by the modification of the exocyclic ring and the metallization of the chromophore. The new functional groups were introduced at 20-position via the Vilsmeier acylation and the Blanc hydroxymethylation. The active structures of chlorin peripheries were oxidized using osmium tetroxide, thaillum nitrate and air as oxidizing agent to introduce the formyl group and the formylmethyl group at 3-, 7-or 12-postion and on the exocyclic ring, respectively. A series of unreported chlorin aldehydes related to chlorophyll were synthesized and their chemical structures were characterized by elemental analysis, UV, IR and 1H NMR spectra. The reaction mechanisms on the hydroformylation for the chlorophyllous chlorins were discussed and the interactions of new compounds with bovine serum albumins were researched.
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