## Abstract The preparation of some aryl‐pyridyl sulphides with potential acaricidal properties is described. In the compounds synthesized the benzene nucleus is substituted with a __para__‐chlorine atom or with three chlorine atoms in positions 2, 4 and 5. Position 5 in the pyridine nucleus is eit
Synthesis and physiological properties of some heterocyclic-aromatic sulphides and sulphones: III Synthesis of some heterocyclic-aromatic sulphones
✍ Scribed by P. A. van Zwieten; M. Gerstenfeld; H. O. Huisman
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 572 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The synthesis of some heterocyclic‐aromatic sulphones with potential acaricidal properties is described. The benzene nucleus in these sulphones is substituted either with a para‐chlorine atom or with three chlorine atoms in positions 2, 4 and 5. The heterocyclic nuclei used are pyridine, pyrimidine, thiazole or thiophen. Apart from the sulphonyl substituent, these nuclei are unsubstituted or carry a halogen substituent; only in the thiophen series a nitro group is substituted in the heterocyclic nucleus. From the aryl‐pyridyl sulphones the corresponding N‐oxydes have been prepared.
📜 SIMILAR VOLUMES
## Abstract The acaricidal properties of some new halogen‐substituted heterocyclic‐aromatic sulphides and sulphones are described. As a rule, the adulticidal activity is negligible, though some compounds show interesting __ovicidal__ properties. The sulphides possess a higher ovicidal activity than
## Abstract The synthesis of some heterocyclic‐aromatic sulphides with potential acaricidal properties is described. The benzene nucleus in these sulphides is substituted either with a __para__‐chlorine atom or with three chlorine atoms in positions 2,4 and 5. The heterocyclic nuclei are pyrimidine