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- Biosynthesis of porphyrins and related macrocycles. Part VII. Synthesis of specifically labelled [14C1]uroporphyrin-III and of [10,14-13C2]uroporphyrin-III. Conversion of the latter into [10,14-13C2]protoporphyrin-IX; biosynthetic significance of its 13C nuclear magnetic resonance spectrum. Alan R. Battersby, Masataka Ihara, Edward McDonald, John Saunders, Robert J. Wells
, J. Chem. Soc., Perkin Trans. 1
, 1976
, 283
- CfbA promotes insertion of cobalt and nickel into ruffled tetrapyrroles in vitro. Ariel E. Schuelke-Sanchez, Alissa A. Stone, Matthew D. Liptak
, Dalton Trans.
, 2020
, 49
, 1065
- Biosynthesis of vitamin B12: derivation of cobyrinic acid from uroporphyrinogen-III. Alan R. Battersby, Masataka Ihara, Edward McDonald, Fumio Satoh, D. Clive Williams
, J. Chem. Soc., Chem. Commun.
, 1975
, 436b
- Biosynthesis of porphyrins and related macrocycles. Part 48.1,2 The rearrangement of 2H-pyrroles (pyrrolenines) related to the proposed spiro-intermediate for porphyrin biosynthesis. Craig J. Hawker, Alan C. Spivey, Finian J. Leeper, Alan R. Battersby
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 1509
- Biobased sunscreen fabrication using Zn-porphyrins from engineered Corynebacterium glutamicum. Young Jin Ko, Jeong-Joo Oh, Sung Ok Han
, Green Chem.
, 2023
, 25
, 5626
- Abiotic formation of uroporphyrinogen and coproporphyrinogen from acyclic reactants. Jonathan S. Lindsey, Vanampally Chandrashaker, Masahiko Taniguchi, Marcin Ptaszek
, New J. Chem.
, 2011
, 35
, 65
- Self-organization of tetrapyrrole constituents to give a photoactive protocell. Ana R. M. Soares, Masahiko Taniguchi, Vanampally Chandrashaker, Jonathan S. Lindsey
, Chem. Sci.
, 2012
, 3
, 1963
- Synthesis of corroles, tetradehydrocorrins, and porphyrins from 1,19-di-iodo- and 19-iodo-1-methyl-1,19-dideoxybiladienes-a,c. Jürgen Engel, Albert Gossauer
, J. Chem. Soc., Chem. Commun.
, 1975
, 713
- Tetrapyrroles: the pigments of life. Alan R. Battersby
, Nat. Prod. Rep.
, 2000
, 17
, 507
- Synthesis of tetradehydrocorrins, corroles, and corrologens related to 12-decarboxyuroporphyrin III and uroporphyrin III. Jurgen Engel, Albert Gossauer, Alan W. Johnson
, J. Chem. Soc., Perkin Trans. 1
, 1978
, 871