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- High-yield synthesis of a chiroporphyrin by hydrogen bond-directed cyclisation. Céline Pérollier, Jacques Pécaut, René Ramasseul, Jean-Claude Marchon, Robert Bau
, Chem. Commun.
, 1999
, 1597
- Intermediates between uroporphyrinogen-1 and coproporphyrinogen-1. Anthony H. Jackson, K. R. Nagaraja Rao, Damrus M. Supphayen, Sydney G. Smith
, J. Chem. Soc., Chem. Commun.
, 1977
, 696
- Biological chemistry. D. F. Elliott, G. S. Marks, A. M. White, C. P. Fawcett, V. H. T. James
, Annu. Rep. Prog. Chem.
, 1962
, 59
, 384
- Synthetic and biosynthetic studies of porphyrins. Part 8. Syntheses of hepta-, hexa-, and penta-carboxylic porphyrins related to uroporphyrin-I. Anthony H. Jackson, Damrus Supphayen
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 277
- The structure of sirohydrochlorin I, a dimethylisobacteriochlorin derived from uroporphyrinogen I. A. Ian Scott, Howard J. Williams, Neal J. Stolowich, Peter Karuso, Mario D. Gonzalez, Francis Blanche, Denis Thibaut, Gerhard Müller, Eleftherios Savvidis, Kersten Hlineney
, J. Chem. Soc., Chem. Commun.
, 1989
, 522
- Porphyrins from a metagenomic library of the marine sponge Discodermia calyx. Rui He, Toshiyuki Wakimoto, Yuya Takeshige, Yoko Egami, Hiromichi Kenmoku, Takuya Ito, Bochu Wang, Yoshinori Asakawa, Ikuro Abe
, Mol. BioSyst.
, 2012
, 8
, 2334
- 13C n.m.r. evidence for a new intermediate, pre-uroporphyrinogen, in the enzymic transformation of porphobilinogen into uroporphyrinogens I and III. Gerardo Burton, Paul E. Fagerness, Shigeki Hosozawa, Peter M. Jordan, A. Ian Scott
, J. Chem. Soc., Chem. Commun.
, 1979
, 202
- Pre-uroporphyrinogen: a substrate for uroporphyrinogen III cosynthetase. Peter M. Jordan, Gerardo Burton, Hans Nordlöv, Monika M. Schneider, Lana Pryde, A. Ian Scott
, J. Chem. Soc., Chem. Commun.
, 1979
, 204
- Recent developments in the chemistry of pyrrolic compounds. K. M. Smith
, Q. Rev. Chem. Soc.
, 1971
, 25
, 31
- Biosynthesis of porphyries and related macrocycles. Part 18. Proof by spectroscopy and synthesis that unrearranged hydroxymethylbilane is the product from deaminase and the substrate for cosynthetase in the biosynthesis of uroporphyrinogen-III. Alan R. Battersby, Christopher J. R. Fookes, Kerstin E. Gustafson-Potter, Edward McDonald, George W. J. Matcham
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 2427