Synthesis and Activity of Juvenile Hormone Analogues (JHA)
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...
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todo:paper_09320776_v43_n8_p1038_Rodriguez2023-10-03T15:48:24Z Synthesis and Activity of Juvenile Hormone Analogues (JHA) Rodriguez, J.B. Gros, E.G. Stoka, A.M. Activity Juvenile Hormone Analogues Synthesis 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. © 1988, Walter de Gruyter. All rights reserved. Fil:Rodriguez, J.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gros, E.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Stoka, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_09320776_v43_n8_p1038_Rodriguez |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Activity Juvenile Hormone Analogues Synthesis |
| spellingShingle |
Activity Juvenile Hormone Analogues Synthesis Rodriguez, J.B. Gros, E.G. Stoka, A.M. Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| topic_facet |
Activity Juvenile Hormone Analogues Synthesis |
| description |
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. © 1988, Walter de Gruyter. All rights reserved. |
| format |
JOUR |
| author |
Rodriguez, J.B. Gros, E.G. Stoka, A.M. |
| author_facet |
Rodriguez, J.B. Gros, E.G. Stoka, A.M. |
| author_sort |
Rodriguez, J.B. |
| title |
Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| title_short |
Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| title_full |
Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| title_fullStr |
Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| title_full_unstemmed |
Synthesis and Activity of Juvenile Hormone Analogues (JHA) |
| title_sort |
synthesis and activity of juvenile hormone analogues (jha) |
| url |
http://hdl.handle.net/20.500.12110/paper_09320776_v43_n8_p1038_Rodriguez |
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AT rodriguezjb synthesisandactivityofjuvenilehormoneanaloguesjha AT groseg synthesisandactivityofjuvenilehormoneanaloguesjha AT stokaam synthesisandactivityofjuvenilehormoneanaloguesjha |
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