Zobrazeno 1 - 4
of 4
pro vyhledávání: '"De-Kai Yuan"'
Autor:
Qingmin Wang, Yongqiang Li, Chi Ming, Xile Deng, Jin Xie, Xinling Yang, Xueping Hu, Li Zhang, De-Kai Yuan
Publikováno v:
Chinese Chemical Letters. 27:566-570
In order to discover highly active ecdysone analogs, a series of new substituted pyrazole amide derivatives were obtained using structure-guided optimization method and further screened for their insecticidal activities, in the basis of the core stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dea172db2d5955f892cee81f89cef90c
https://doi.org/10.1016/j.cclet.2016.02.009
https://doi.org/10.1016/j.cclet.2016.02.009
Publikováno v:
Chinese Chemical Letters. 23:669-672
In order to investigate the biological activity of novel bis-pyrazole compounds, a series of N-(3-alkyl-5-(N-methylcarbamyl)-1H-pyrazol-4-yl)-3-alkyl-4-substituted-1H-pyrazole-5-carboxamides were designed and synthesized with ethyl 3-alkyl-1H-pyrazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::782356e0b7a293b13ca8efffdebff2a1
https://doi.org/10.1016/j.cclet.2012.04.010
https://doi.org/10.1016/j.cclet.2012.04.010
Publikováno v:
ChemInform. 34
Pyrazolo[3,4- b]pyridines have been obtained by the condensation of 5-amino-4-cyanopyrazole, readily available by the reaction of dithioacetals with substituted hydrazines, with β-ketoesters or β-diketone in the presence of tin(IV) chloride at refl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea4553ce2f75fb1ac589374f08c1663
https://doi.org/10.1002/chin.200305164
https://doi.org/10.1002/chin.200305164
Publikováno v:
Chinese Chemical Letters. 18:915-916
Six novel 12-alkoxycarbonylmethylene-1,15-pentadecanolides ( 3 ) were synthesized from 2-nitrocyclo-dodecanone by the Michael addition with acrolein followed by ring enlargement, Nef reaction and Wittig–Horner reaction. Their structures were confir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47be04727fad334407dd9e320c56373e
https://doi.org/10.1016/j.cclet.2007.05.042
https://doi.org/10.1016/j.cclet.2007.05.042