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Imino [4+4] cycloaddition products as exclusive and biologically relevant acrolein-amine conjugates are intermediates of 3-formyl-3,4-dehydropiperidine (FDP), an acrolein biomarker
Takamatsu M., Fukase K., Kurbangalieva A., Tanaka K.
of the reaction, through an imino [4+4] cycloaddition, of biologically relevant amines with acrolein
Unrecognized Cycloaddition Reactions of N-Alkyl-α,β-Unsaturated Imines Occurring in Biosystems and Their Biological Roles
Pradipta A., Tsutsui A., Latypova L., Chulakova D., Smirnov I., Kurbangalieva A., Tanaka K.
, hexahydropyrimidines, and 1,3,5-triazacyclooctanes via formal [4 + 4], [4 + 2], and [4 + 2 + 2] cycloadditions in a
Imino [4+4] cycloaddition products as exclusive and biologically relevant acrolein-amine conjugates are intermediates of 3-formyl-3,4-dehydropiperidine (FDP), an acrolein biomarker
Takamatsu M., Fukase K., Kurbangalieva A., Tanaka K.
of the reaction, through an imino [4+4] cycloaddition, of biologically relevant amines with acrolein
Exclusive formation of imino[4 + 4]cycloaddition products with biologically relevant amines: Plausible candidates for acrolein biomarkers and biofunctional modulators
Tsutsui A., Pradipta A., Saigitbatalova E., Kurbangalieva A., Tanaka K.
of the reaction of acrolein with biologically relevant amines via an imino[4 + 4]cycloaddition. These compounds
Exclusive formation of imino[4 + 4]cycloaddition products with biologically relevant amines: Plausible candidates for acrolein biomarkers and biofunctional modulators
Tsutsui A., Pradipta A., Saigitbatalova E., Kurbangalieva A., Tanaka K.
of the reaction of acrolein with biologically relevant amines via an imino[4 + 4]cycloaddition. These compounds
Unrecognized Cycloaddition Reactions of N-Alkyl-α,β-Unsaturated Imines Occurring in Biosystems and Their Biological Roles
Pradipta A., Tsutsui A., Latypova L., Chulakova D., Smirnov I., Kurbangalieva A., Tanaka K.
, hexahydropyrimidines, and 1,3,5-triazacyclooctanes via formal [4 + 4], [4 + 2], and [4 + 2 + 2] cycloadditions in a
Insight into the reaction mechanism and chemoselectivity in the cycloaddition of ynamides and isoxazoles with H2O
Zhou L., Yang L., Dai S., Gao Y., Fang R., Kirillov A.M., Yang L.
The mechanism and chemoselectivity in the cycloaddition of ynamides and isoxazoles have been
Novel cyano-activated Cu(ii) complexes of arylhydrazones of active methylene nitriles and their catalytic application for azide-alkyne cycloaddition in water and glycerol
Gurbanov A.V., Mahmoud A.G., Aliyeva V.A., Guedes da Silva M.F.C., Pombeiro A.J.L.
)(py)]n (4), respectively, where (L1a)2− = (Z)-1-(2-carboxylatophenyl)-2-(1-cyano-2-imino-2-methoxyethylidene
Perhydrofuro[3,2-c]-, perhydropyrano[3,2-c]-, and 4-ethoxy-2-(5-R-furan-2- yl)tetrahydroquinolines. Synthesis and transformations
Zubkov F.I., Zaitsev V.P., Piskareva A.M., Eliseeva M.N., Nikitina E.V., Mikhailova N.M., Varlamov A.V.
- [3,2-c]quinolines, and 4-ethoxyquinolines were synthesized by the imino Diels-Alder (Povarov
EFFICIENT SYNTHESIS OF IMINO-1,3-THIAZINAN-4-ONE PROMOTED BY ACETONITRILE ELECTROGENERATED BASE AND COMPUTATIONAL STADIES WITH CB1 AND 11 βHSD1 MOLECULES
Sbei N., Titov A.A., Voskressensky L.G.
EFFICIENT SYNTHESIS OF IMINO-1,3-THIAZINAN-4-ONE PROMOTED BY ACETONITRILE ELECTROGENERATED BASE

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