Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Yu. A. Baskakov"'
Publikováno v:
Photosynthesis: from Light to Biosphere ISBN: 9789401065627
Photosynthesis: from Light to Biosphere
Photosynthesis: from Light to Biosphere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f88f1ae65b42f9417642788d1cd1fb1
https://doi.org/10.1007/978-94-009-0173-5_104
https://doi.org/10.1007/978-94-009-0173-5_104
Publikováno v:
Journal of Engineering Physics. 29:1364-1367
Results are presented on film cooling by homogeneous injection into a turbulent boundary layer through porous inserts of various lengths along the main flow direction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91d74ac5d486c5f9c050810efb422598
https://doi.org/10.1007/bf00858164
https://doi.org/10.1007/bf00858164
Autor:
Yu. A. Baskakov, S. P. Epshtein, T. G. Simonova, V. P. Tashchi, Yu. G. Putsykin, A. F. Rukasov
Publikováno v:
Chemistry of Heterocyclic Compounds. 19:74-78
The reaction of N1-or N2-monoacyl derivatives of 2-hydrazinocyclohexanone, 3-hydrazino-3-methyl-2-butanone, and 2-hydrazino-2-methylpropanal oximes with isocyanates was used to synthesize, N,N-diacyl derivatives, which, under the influence of acids o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d27f667b69e0440e26dac90da360e83
https://doi.org/10.1007/bf00512820
https://doi.org/10.1007/bf00512820
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:761-764
Treatment of 2-ethylamino-2-methylpropanol oxime with aryl isocyanates leads to 4-[N-(arylcarbamoyl) hydroxyamino [-1-ethyl-3-aryl-5,5-dimenthyl-2-imidazolidionones, which are acylated by acid chlorides and methyl isocyanate to give the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47c6b266e8a08905c34b7d631d1fd0d0
https://doi.org/10.1007/bf00557756
https://doi.org/10.1007/bf00557756
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:1039-1044
4-Hydroxy- and 4-hydroxylamino-1-hydroxy-3-aryl-5,5-dimethyl-2-imidazolidinones, respectively, were obtained by treatment of N-arylcarbamoyl derivatives of N-(1-oximino-2-methyl-2-porpyl)hydroxylamine with acids and alkalis. 4-Hydroxylaminoimidazolid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19d173992c324dc974fe38e8d2f83120
https://doi.org/10.1007/bf00480403
https://doi.org/10.1007/bf00480403
Publikováno v:
Chemistry of Heterocyclic Compounds. 22:1084-1087
Interaction of nitrosyl chloride with 1-arylimidazolin-2-ones in methanol leads to the formation of 4,5-dimethyoxyimidazolidin-2-ones. Under similar conditions 1,5-diarylimidazolin-2-ones give 1,5-diaryl-4-oximino-5-alkoxyimidazolidin-2-ones. When th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::680ea59f98e70dc0fc02f8ff42cf375f
https://doi.org/10.1007/bf00473483
https://doi.org/10.1007/bf00473483
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:603-607
The reaction of 5-hydroxy-3,3,5-trimethylisoxazolidine with alkyl (or aryl) isocyanates gives N-alkyl(aryl)-carbamoyl-5-hydroxy-3,3,5-trimethylisoxazolidines, which react with methanol in the presence of p-toluenesulfonic acid to give 5-methoxy-1-car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15e6b64199a20177d37e6f4c47d124f6
https://doi.org/10.1007/bf00539492
https://doi.org/10.1007/bf00539492
Autor:
Yu. A. Baskakov
Publikováno v:
Pesticide Science. 4:289-303
Acylhydroxylamines have attracted general attention following the successful development of the highly-efficient linuron group herbicides1 and a search for new herbicides from among this class of compounds has led to the development of three new grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91da59edcde6f8bb48e3077771f72c4f
https://doi.org/10.1002/ps.2780040306
https://doi.org/10.1002/ps.2780040306
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:115-118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e76af61052d86981174055799c946a35
https://doi.org/10.1007/bf00478506
https://doi.org/10.1007/bf00478506
Publikováno v:
Chemistry of Heterocyclic Compounds. 7:226-229
The prototropic transformation of O-(N′-methylcarbamidomethyl)-N-carboisopropoxy-N-phenylhydroxylamine in the presence of sodium ethoxide to form isopropyl phenylcarbamate, N-phenyl-N′-methylurea, and glyoxylic acid derivatives was studied. A sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79424f69306fe1e9bbb75d5be089a68a
https://doi.org/10.1007/bf00473094
https://doi.org/10.1007/bf00473094