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Journal ArticleDOI

Stereochemistry of biosynthesis of the vinyl groups of protoporphyrin-IX: a short synthesis of porphobilinogen

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TLDR
Porphobilinogen (1), [2H]-labelled in the propionic residue, is synthesised by a short route and is used to establish that both vinyl groups of protoporphyrin-IX are biosynthesised by overall antiperiplanar elimination of a proton and carbon dioxide.
Abstract
Porphobilinogen (1), [2H]-labelled in the propionic residue, is synthesised by a short route and is used to establish that both vinyl groups of protoporphyrin-IX are biosynthesised by overall antiperiplanar elimination of a proton and carbon dioxide.

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Structure and function of enzymes in heme biosynthesis.

TL;DR: This review summarizes the current understanding of the structure–function relationship for all heme biosynthetic enzymes and their potential interactions in the cell.
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Prokaryotic Heme Biosynthesis: Multiple Pathways to a Common Essential Product.

TL;DR: Diversity in the regulation of these pathways reflects the diversity of bacterial metabolism and has significantly slowed advances in this field such that no single organism's heme synthesis pathway regulation is currently completely characterized.
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A new approach to porphobilinogen and its analogs

TL;DR: The van Leusen pyrrole synthesis was used to assemble three potential precursors of porphobilinogen, one of which was converted to the natural product using a new method for the direct alkylation of β-hydroxymethylpyrroles.
Journal ArticleDOI

A General Method for the Preparation of 4- and 6-Azaindoles

TL;DR: Nitropyridines reacted with an excess of vinyl Grignard reagent to produce 4- or 6-azaindoles and improved yields were obtained when a halogen atom was present at the position alpha to the nitrogen atom in the pyridine ring.
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