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- Non-aryl substituted aza-BODIPYs at 1,7- or 3,5-sites: synthesis, structures, optical properties, and applications. Dongxiang Zhang, Guorui Liu, Xin-Dong Jiang
, J. Mater. Chem. C
, 2023
, 11
, 1668
- Pyrroles and related compounds. Part XXVII. Syntheses of porphyrins with a nuclear carboxy-group. T. Trefor Howarth, Anthony H. Jackson, George W. Kenner
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 502
- Pyrroles and related compounds. Part XIX. Synthesis of phylloporphyrins related to chlorobium chlorophyll (660). M. T. Cox, A. H. Jackson, G. W. Kenner
, J. Chem. Soc. C
, 1971
, 1974
- Synthesis of aza-BODIPYs with barrier-free rotation of the –tBu group at 3-site and enhancement of photothermal therapy by triggering cancer cell apoptosis. Junzhu Zhao, Huan Wang, Dongxiang Zhang, Yue Shen, Shan Zhang, Junyi Ren, Zhan Wang, Ya-nan Sun, Jianjun Du, Xin-Dong Jiang, Guiling Wang
, J. Mater. Chem. B
, 2022
, 10
, 8443
- Synthesis and characterisation of the C30-de-ethylaetioporphyrin present in petroleum. Paul J. Clewlow, Anthony H. Jackson
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1925
- Maleimide index: a paleo-redox index based on fragmented fossil-chlorophylls obtained by chromic acid oxidation. Kenta Asahina, Satoshi Takahashi, Ryosuke Saito, Kunio Kaiho, Yasuhiro Oba
, RSC Adv.
, 2022
, 12
, 31061
- Pyrroles and related compounds. Part XV. Differential protection of pyrrole rings during porphyrin synthesis. Syntheses of mesoporphyrin-XI. P. J. Crook, A. H. Jackson, G. W. Kenner
, J. Chem. Soc. C
, 1971
, 474
- Synthetic approaches to versatile hemoprotein model compounds built from porphyrins and peptides. Anthony H. Jackson, George W. Kenner, Kevin M. Smith, Colin J. Suckling
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 1441
- Synthetic studies relevant to biosynthetic research on vitamin B12. Part 2. Syntheses of C-methylated chlorins via lactams. Alan R. Battersby, Christopher J. R. Fookes, Roger J. Snow
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 2733
- 56. 2,2′-Bipyrroles. R. Grigg, A. W. Johnson, J. W. F. Wasley
, J. Chem. Soc.
, 1963
, 359