Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yu. N. Firsova"'
Autor:
S. R. Engel, S. E. Sosonyuk, Nikolay S. Zefirov, N. A. Lozinskaya, Yu. N. Firsova, Marina V. Proskurnina
Publikováno v:
Russian Chemical Bulletin. 64:76-82
The preparative procedure for the synthesis of N-(2,2,2-trichloro-1-hydroxyethyl)aldimines from the corresponding aldehyde, chloral, and ammonium acetate was developed. Preparative silylation and acylation of their hydroxy groups were acomplished for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::586c8f1d8af26e86cfd2ae489fcacd02
https://doi.org/10.1007/s11172-015-0823-8
https://doi.org/10.1007/s11172-015-0823-8
Publikováno v:
Review Journal of Chemistry. 2:74-104
The key role of imines in organic synthesis, for example in the synthesis of amine derivatives and nitrogen heterocycles, is well known. However, the instability of N-unsubstituted imines is often an obstacle to the selection of synthesis strategy. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddae30540c73083e187bc393429773fd
https://doi.org/10.1134/s2079978012010037
https://doi.org/10.1134/s2079978012010037
Publikováno v:
Russian Chemical Bulletin. 60:1989-1994
1-Arylideneamino-2,2,2-trichloroethanols react regiospecifically with cyclopropenones to form 2,2′-diaryl-1,1′,2,2′-tetrahydro-3H,3′H-2,2′-bipyrrole-3,3′-diones. A new preparative method was developed for the synthesis of 1-arylideneamino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c408a5cbe607b6633ef29bcaa19610bd
https://doi.org/10.1007/s11172-011-0301-x
https://doi.org/10.1007/s11172-011-0301-x
Publikováno v:
Russian Chemical Bulletin. 58:152-155
N,N’-Bis(arylidene)methanediamines regiospecifically react with 2,3-diphenylcyclo- propenone to form stable adducts of both the mono- and the diaddition. Ammonium acetate serves as the catalyst of the process. During hydrolysis of these adducts, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::408cffaf483c099bdbf60201f4acbbf6
https://doi.org/10.1007/s11172-009-0023-5
https://doi.org/10.1007/s11172-009-0023-5
Autor:
Yu. N. Firsova, Alexander D. Ryabov
Publikováno v:
Russian Chemical Bulletin. 46:1700-1706
The effect of micelles of different surfactants (cationic, anionic, and neutral) on the kinetics of the glucose oxidase-catalyzed reduction of ferrocenium cations RFc+ (R=H, Bun) byd-glucose was studied by spectrophotometry. In micellar media of Trit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e74202cd8c854952944a29229ca70b3
https://doi.org/10.1007/bf02495119
https://doi.org/10.1007/bf02495119
Publikováno v:
ChemInform. 43
The title compounds (III) and (VII) react regiospecifically with cyclopropanones to give 2,2′-diaryl-tetrahydrobipyrrole-3,3′-dione derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::896a0605153d282270a9bf2ae64acd11
https://doi.org/10.1002/chin.201247095
https://doi.org/10.1002/chin.201247095
Publikováno v:
ChemInform. 41
Diamines (II) react regiospecifically with cyclopropenone (I) to form exclusively stable adducts of both mono- and diaddition depending on the educt ratio.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f1bee7ef3f0356de917412a59d8b7b6
https://doi.org/10.1002/chin.201032120
https://doi.org/10.1002/chin.201032120