Zobrazeno 1 - 10
of 169
pro vyhledávání: '"N. Pronayova"'
Autor:
Kristína Plevová, Anton Gatial, N. Pronayova, Pavel Matějka, Viktor Milata, Sandra Dorotíková
Publikováno v:
Journal of Molecular Structure. 1090:112-120
The isomers and conformers of push–pull 3-fluorophenylamino-2-acetyl propenenitrile (FH4C6) NH CH C(CN)(COCH3) (FPAAPN) have been studied experimentally by NMR and vibrational spectroscopy and theoretically by ab initio calculations at MP2 and DFT
Autor:
Jozef Kožíšek, Anton Gatial, M. Gróf, N. Pronayova, H. Juhásová, Pavel Matějka, Viktor Milata
Publikováno v:
Journal of Molecular Structure. 993:232-242
The isomers and conformers of four push–pull compounds: methyl-2-cyano-3-methoxyacrylate (MCMA) H3C O CH C(CN)(COOCH3), methyl-2-cyano-3-aminoacrylate (MCAA) H2N CH C(CN)(COOCH3), methyl-2-cyano-3-methylaminoacrylate (MCMAA) H3C NH CH C(CN)(COOCH3)
Autor:
Anton Gatial, Martin Breza, Viktor Milata, Pavel Matějka, N. Pronayova, M. Gróf, Jozef Kožíšek
Publikováno v:
Journal of Molecular Structure. 938:97-110
The IR, Raman and NMR spectra of 3-N,N-dimethylhydrazino-2-acetyl propenenitrile (DMHAP) [(H3C)2N NH CH C(CN)(COCH3)] were measured. X-ray analysis revealed that DMHAP exists in solid state as ZZa conformer. Vibrational and NMR spectra confirmed the
Publikováno v:
Journal of Molecular Structure. :54-61
The IR and Raman spectra of aminomethylene-malonic acid dimethylester (AMDME) [NH 2 CH C(COOCH 3 ) 2 ] and its N -methyl derivatives (MAMDME and DMAMDME) were measured in solid phase and in different solvents at various temperatures. X-ray analysis r
Autor:
Anton Gatial, Martin Breza, Pavel Matějka, Viktor Milata, Jozef Kožíšek, N. Pronayova, M. Gróf
Publikováno v:
Journal of Molecular Structure. 891:192-204
The IR, Raman and NMR spectra of 3- N , N -dimethylhydrazino-2-methylsulfonyl propenenitrile (DMHSP) [(H 3 C) 2 N NH CH C(CN) (SO 2 CH 3 )] as a solid and in different solvents were measured. The spectra and X-ray analysis revealed that DMHSP was pre
Publikováno v:
ARKIVOC, Vol 2001, Iss 2, Pp 109-121 (2001)
The nitrones derived from cyclic acetals of D-erythrose 1a,b and D-threose 2a,b react with N- phenylmaleimide (3) to afford the corresponding diastereomeric isoxazolidines. The stereoselectivity is dependent on the steric hindrance of the nitrone. In
Autor:
Peter Baran, Martin Breza, Guido Kickelbick, N. Pronayova, Peter Šafář, Jozef Kožíšek, František Považanec
Publikováno v:
Scopus-Elsevier
5-[(2-Furyl)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione (1a) treated with equimolar amount of pyrrolidine or hexahydroazepine afforded 5-(pyrrolidine)- (2a) or 5-[(hexahydro- azepine-1-yl)-2-hydroxypenta-2,4-dien-1-ylidene]-2,2-dimethyl-1,3-dioxa
Publikováno v:
Collection of Czechoslovak Chemical Communications. 62:1105-1113
(5-Bromo-2-furyl)methylidenemalonodinitrile (1) reacted with substituted aromatic amines under formation of (5-N-arylamino-2-furyl)methylidenemalonodinitriles 2a-2h whereas no reaction was observed with N-alkyl-N-phenylamines. Derivatives of 2-cyano-
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:371-380
Nucleophilic reaction of 5-amino- and 6-amino-2-substituted benzoxazoles 1 and 2 with 3-ethoxymethylene-2,4-pentanedione (3) gave compounds 5 and 6. Compounds 1 and 2 reacted with ethyl ethoxymethylene-3-oxobutanoate (4) under formation of compounds
Publikováno v:
Collection of Czechoslovak Chemical Communications. 60:605-611
Condensation reactions of 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinecarbaldehyde with nine acid derivatives containing an active methylene group are described. The obtained products were characterized by their IR, UV, 1H NMR, 13C NMR and mass