Absolute Stereochemistry of Precorrin-3x and Its Relevance to the Dichotomy of Ring Contraction Mechanism in Vitamin B12 Biosynthesis
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (7), 1657-1662
- https://doi.org/10.1021/ja952739s
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- On the Duality of Mechanism of Ring Contraction iv Vitamin B12 BiosysthesisHETEROCYCLES, 1994
- Biosynthesis of vitamin B12: ring contraction is preceded by incorporation of molecular oxygen into precorrin-3Journal of the American Chemical Society, 1993
- Isolation, structure, and genetically engineered synthesis of precorrin-5, the pentamethylated intermediate of vitamin B12 biosynthesisJournal of the American Chemical Society, 1993
- Biosynthesis of vitamin B12FEBS Letters, 1993
- Biosynthesis of vitamin B12: structure of precorrin-3B, the trimethylated substrate of the enzyme catalysing ring contractionJournal of the Chemical Society, Chemical Communications, 1993
- A facile synthesis of δ‐aminolevulinic acid (ALA) regioselectively labeled with13C and direct observation of enzymatic transformation from ALA to porphobilinogen (PBG)Journal of Labelled Compounds and Radiopharmaceuticals, 1989
- Studies on the biosynthesis of corrinoids and porphyrinoids. I. The labeling of oxygen of vitamin B12.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- Improved spectral resolution in COSY 1H NMR spectra of proteins via double quantum filteringBiochemical and Biophysical Research Communications, 1983
- Application of phase sensitive two-dimensional correlated spectroscopy (COSY) for measurements of 1H-1H spin-spin coupling constants in proteinsBiochemical and Biophysical Research Communications, 1983
- Oxygen-18 isotope effect in carbon-13 nuclear magnetic resonance spectroscopy. 2. The effect of structureJournal of the American Chemical Society, 1980