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'cyclodien insecticides' in keywords
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1979 (1)
1973 (1)
1Author    K. Hustert, J. Schmitzer, H. Parlar, F. KörteRequires 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 
2Author    Michael Perscheid, H. Orst Schlüter, Karlheinz BallschmiterRequires 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