JOURNAL ARTICLE

Synthesis of [4′‐13C] pyridoxol

V. W. Vande VeldeNeil E. MackenzieA. Ian Scott

Year: 1985 Journal:   Journal of Labelled Compounds and Radiopharmaceuticals Vol: 22 (6)Pages: 595-606   Publisher: Wiley

Abstract

Abstract 5‐Cyano‐3‐hydroxy‐2‐methylpyridine‐l‐oxide, after O‐methylation with dimethylsulfate, was reacted regiospecifically with sodium [ 13 C] cyanide to give [4′‐ 13 C] 4,5‐dicyano‐3‐hydroxy‐2‐methylpyridine. The latter compound was successively transformed to [4′‐ 13 C] pyridoxol and [4′‐ 13 C] pyridoxal phosphate.

Keywords:
Chemistry Cyanide Sodium cyanide Medicinal chemistry Sodium Stereochemistry Nitrile Organic chemistry

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Citation History

Topics

Enzyme Structure and Function
Physical Sciences →  Materials Science →  Materials Chemistry
Chromatography in Natural Products
Physical Sciences →  Chemistry →  Analytical Chemistry
Glycosylation and Glycoproteins Research
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Molecular Biology

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