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Chemotherapie der experimentellen Tuberkulose II. Kernsubstituierte Isonicotinsäurehydrazide

✍ Scribed by O. Isler; H. Gutmann; O. Straub; B. Fust; E. Böhni; A. Studer

Publisher: John Wiley and Sons
Year: 1955
Tongue: German
Weight: 957 KB
Volume: 38
Category: Article
ISSN: 0018-019X
DOI: 10.1002/hlca.19550380424

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✦ Synopsis

Abstract

Some twenty‐six isonicotinic acid hydrazides substituted in the pyridine ring by hydrocarbon groups or by functional substituents, such as hydroxy, chlorine, alkoxy, and amino, were synthesized according to conventional methods and tested for their antitubercular action.

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Chemotherapie der experimentellen Tuberkulose III. Derivate des 2-Methyl-isonicotinsäurehydrazids

✍ O. Isler; H. Gutmann; O. Straub; B. Fust; E. Böhni; A. Studer 📂 Article 📅 1955 🏛 John Wiley and Sons 🌐 German ⚖ 999 KB

## Abstract Some fifty‐two derivatives of 2‐methylisonicotinic acid hydrazide were synthesized and tested for their antitubercular action. The derivatives were prepared by reaction of 2‐methylisonicotinic acid hydrazide with aldehydes, ketones, and carboxylic acid chlorides, by condensation of 2‐me