| 1 | Author
| K. Hustert, J. Schmitzer, H. Parlar, F. Körte | Requires cookie* | | Title
| Zur Synthese von 2.5-und 2.6-verbrückten Tetrahydromethanoindanen Synthesis of 2,5-and 2,6-Crosslinked Tetrahydromethanoindanes  | | | Abstract
| A direct synthetic method for some 2,5-and 2.6-crosslinked chlorinated tetrahydromethano-indanes, which are the most important conver-sion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and m NMR. | | |
Reference
| Z. Naturforsch. 34b, 525—527 (1979); eingegangen am 7. Dezember i978 | | |
Published
| 1979 | | |
Keywords
| Cyclodien Insecticides, UV Photolysis, Cross-linked Chlorinated Tetrahydromethanoindanes | | |
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| | | | TEI-XML for
| default:Reihe_B/34/ZNB-1979-34b-0525_n.pdf | | | Identifier
| ZNB-1979-34b-0525_n | | | Volume
| 34 | |
2 | Author
| Michael Perscheid, H. Orst Schlüter, Karlheinz Ballschmiter | Requires cookie* | | Title
| Aerober Abbau von Endosulfan durch Bodenmikroorganismen Aerobic D egradation of Endosulfan by Microorganisms  | | | Abstract
| Microbial degradation of both the isomers of the cyclodiene insecticide endosulfan (hexachloro-bicyclo [2,2,1] hept-5-en-2,3-bis-hydroyxmethylene-cyclic sulfit) by Pseudomonadaceae in water has been investigated. Strong resorption of the applied insecticide (90%) by the bacteria has been ob served. The main metabolite of both the isomers was identified by EC-gaschromatography as the endosulfan-alcohol. Additionally the /?-isomere yielded small amounts of the cyclic endosulfan-ether and isomerisation to the more stable a-endosulfan. | | |
Reference
| (Z. Naturforsch. 28c, 761—763 [1973]; eingegangen am 25. Juli 1973) | | |
Published
| 1973 | | |
Keywords
| Endosulfan, biodegradation, microorganisms, Pseudomonas, cyclodien-insecticides | | |
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| | | | TEI-XML for
| default:Reihe_C/28/ZNC-1973-28c-0761.pdf | | | Identifier
| ZNC-1973-28c-0761 | | | Volume
| 28 | |
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