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1988 (1)
1Author    JuanB. Rodriguez, EduardoG. Gros, AngelM. StokaRequires cookie*
 Title    Synthesis and Activity of Juvenile Hormone Analogues (JHA)  
 Abstract    From geranylacetone and by the use of a variety of reagents, twelve analogues of the juvenile hormone III were synthesized. The compounds (5—16) have an isoprenic structure bearing at the extreme of the chain functional groups as carbonate, carbamate, thiolcarbonate, thiolcarbamate, carbonyloxyimino and thiol carbonyloxyimino. Compounds 5—9 present the normal unsaturated isoprenic chain while compounds 10—16 have a monoepoxide function. All the compounds were tested for their respective juvenile hormone activity for Triatoma infestans and Rhodniusprolixus. The most active compounds were those having a thiol carbonate group independently of the oxidation state of the molecule. The synthetic procedures and the biological results are discussed. 
  Reference    Z. Naturforsch. 43b, 1038—1042 (1988); received March 8. 1988 
  Published    1988 
  Keywords    Juvenile Hormone Analogues, Activity, Synthesis 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-1038.pdf 
 Identifier    ZNB-1988-43b-1038 
 Volume    43