Issue 7, 1979

Biosynthesis of the natural porphyrins: experiments on the ring-closure steps and with the hydroxy-analogue of porphobilinogen

Abstract

Experiments on the conversion of porphobilinogen PBG (1) into uro'gens support formation of the pyrrolenine (4) which, at least for production of uro'gen-I (9), is converted next into the hydroxymethylbilane (6); the status of the latter for uro'gen-III (10) formation and the nature of the interaction between deaminase and cosynthetase are also studied.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 316-319

Biosynthesis of the natural porphyrins: experiments on the ring-closure steps and with the hydroxy-analogue of porphobilinogen

A. R. Battersby, C. J. R. Fookes, G. W. J. Matcham, E. McDonald and K. E. Gustafson-Potter, J. Chem. Soc., Chem. Commun., 1979, 316 DOI: 10.1039/C39790000316

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