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Synthesis of Long-chain 1-Alkylimidazole-2-thiols, 1-Alkylimidazoles, and Some Related Benzimidazole Compounds

✍ Scribed by Bäuerlein, Edmund ;Trasch, Heinz


Book ID
102899627
Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
521 KB
Volume
1979
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

This article describes the synthesis of long‐chain 1‐alkylimidazole‐2‐thiols 3 and 1‐decylbenzimidazole‐2‐thiol (10), of value as nucleophilic scavengers for sulfenyl groups (RS^+^) in lipophilic membranes^2)^ and as inhibitors of thyroid peroxidase^3)^, as well as of the corresponding 1‐alkylimidazoles 6 and ‐benzimidoles 7. Because 1‐decyl compounds belonging to the benzimidazole series apparently have a specific action on proton translocation in the mitochondrial system, which depends on their basicity^2)^., the half‐neutralisation potentials of 7c, 10 and 11 have been determined in aqueous acetonitrile.


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Synthesis of isotopically labelled 1,1′-
✍ J. M. Harrison 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 French ⚖ 215 KB 👁 1 views

## Abstract 1,1′‐Thiobis (2‐hydroxyethane) has been synthesized isotopically labelled with sulphur‐35, carbon‐13 and deuterium. The conversion to 1,1′‐thiobis (2‐chloroethane) labelled with sulphur‐35 and carbon‐13 is described.