Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Tibor Timar"'
Publikováno v:
Journal of Heterocyclic Chemistry. 52:1677-1683
4,4-Dimethylchromeno[4,3-d]selenadiazoles 8 with insecticide activities have been synthesized via oxidative ring closure of the corresponding semicarbazone derivatives 7 by treatment with selenium dioxide. Reaction of various alkoxy-2,2-dimethyl-2H-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e1c0d57cad35a08881ad4027d983a95
https://doi.org/10.1002/jhet.2247
https://doi.org/10.1002/jhet.2247
Publikováno v:
Journal of Heterocyclic Chemistry. 37:1389-1417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::942a8d68af3748511a5c479a7ecbcb87
https://doi.org/10.1002/jhet.5570370602
https://doi.org/10.1002/jhet.5570370602
Publikováno v:
Archives of Insect Biochemistry and Physiology. 32:493-501
The precocenes have notable effects on insect development, in particular they can induce specific destruction of corpora allatal cells and thus prevent the synthesis of juvenile hormones. As juvenile hormones have wide-ranging physiological roles in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4eb206a43d13463fe2e0a1860654128
https://doi.org/10.1002/(sici)1520-6327(1996)32:3/4<493::aid-arch21>3.0.co
https://doi.org/10.1002/(sici)1520-6327(1996)32:3/4<493::aid-arch21>3.0.co
Publikováno v:
The Journal of Organic Chemistry. 61:5375-5383
Competitive α and β cyclization of 2‘-hydroxychalcone epoxides affords 2-(α-hydroxybenzyl)-3-coumaranone and/or 3-hydroxyflavanones, which depends on the conditions employed. Epoxidation of 2‘-hydroxychalcones by dimethyldioxirane followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fd38c175bb3258c8f1f14db954b77f7
https://doi.org/10.1021/jo960163z
https://doi.org/10.1021/jo960163z
Publikováno v:
Archives of Insect Biochemistry and Physiology. 30:25-40
The relationship between the structure of nineteen 2,2-dimethylchromene derivatives and their effects on aphid morphogenesis were investigated in a pink clone of the pea aphid, Acyrthosiphon pisum (Harris). Three bioassay systems were used: (1) wing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46c2c9f27252c32fef1f1b42b3722b7e
https://doi.org/10.1002/arch.940300103
https://doi.org/10.1002/arch.940300103
Publikováno v:
The Journal of Organic Chemistry. 59:6318-6321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ef36c7191b977ee78365ad2b889c795
https://doi.org/10.1021/jo00100a038
https://doi.org/10.1021/jo00100a038
Publikováno v:
Synthesis. 1994:837-840
A new and expeditious synthesis of 7-alkylthio-2,2-dimethyl-2H-chrome- nes in good overall yield (59-72%), utilising the Newman-Kwart rearran- gement of 7-(N,N-dimethylthiocarbamoyloxy)-2,2-dimethyl-4-chromanones as the key step, is described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcd729e73cddb4b75fc232603719cad8
https://doi.org/10.1055/s-1994-25585
https://doi.org/10.1055/s-1994-25585
Publikováno v:
Journal of Pesticide Science. 18:277-280
2,2-ジメチル-4H-[1] ベンゾピラノ [4,3-d][1,2,3] セレンジアゾール類 (I) と2,2-ジメチル-3,4-ジクロロクロメン類 (II) のオオモンシロチョウとコロラドハムシに対する殺幼虫活性を調べた. (I) と
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fb0f4d4e4461c7f3aab65ab32d883c4
https://doi.org/10.1584/jpestics.18.3_277
https://doi.org/10.1584/jpestics.18.3_277
Publikováno v:
Journal of Agricultural and Food Chemistry. 41:148-152
5-(Arylmethylene)hydantoins (4-19) and 5-(arylmethylene)-2-thiohydantoins (20-37) have been synthesized by condensation of aromatic aldehydes with hydantoin (1) or 2-thiohydantoin (2) in the presence of ethanolamine. A number of 5-alkyl- and 5-(arylm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc81ed9b205285ce288ce88d6fc49a8b
https://doi.org/10.1021/jf00025a031
https://doi.org/10.1021/jf00025a031
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98b4831112da65366eaf0fd671064fdc
https://doi.org/10.1002/chin.199107049
https://doi.org/10.1002/chin.199107049