Isomerization of uroporphyrinogen I octamethyl ester through spiro-pyrrolenine intermediate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. 2-Mercaptobenzothiazolylmethylpyrrole as a new means for the synthesis of pyrromethanes under neutral conditions
2. Biosynthesis of the pigments of life: mechanistic studies on the conversion of porphobilinogen to uroporphyrinogen III
3. Mechanistic and evolutionary aspects of vitamin B12 biosynthesis
4. 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
5. Biosynthesis of porphyrins and related macrocycles. Part VIII. Enzymic decarboxylation of uroporphyrinogen-III: structure of an intermediate, phyriaporphyrinogen-III, and synthesis of the corresponding porphyrin and of two isomeric porphyrins
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. New dimensions in calix[4]pyrrole: the land of opportunity in supramolecular chemistry;RSC Advances;2019
2. Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at β-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogens;Org. Biomol. Chem.;2003
3. Studies on the tetramerization of substituted monopyrroles to type I porphyrins;Tetrahedron Letters;2002-09
4. meso-Unsubstituted Porphyrinogens and Hexaphyrinogens: The First X-ray Characterization;Journal of the American Chemical Society;2000-06-27
5. Synthesis of a linear α-hydroxymethyl-pentapyrrole derivative and its cyclization to uroporphyrinogens;Tetrahedron Letters;2000-04
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