Synthesis and characterization of 2,2-disubstituted thiadiazolines

Autor: M. A. Martins Alho, Beatriz N. Brousse, Albertina G. Moglioni, Norma D´Accorso, Graciela Y. Moltrasio
Jazyk: angličtina
Rok vydání: 2000
Předmět:
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1
3
4 thiadiazoline
Hydrogen
5 methoxyindan 1 one thiosemicarbazone
Chemical structure
Heteroatom
6 methoxyindan 1 one thiosemicarbazone
chemistry.chemical_element
spiro[5 acetamido 3 n acetyl 2
1' (5' methoxyindan)] 1
3
4 thiadiazoline
Mass spectrometry
proton nuclear magnetic resonance
4 methoxybenzophenone thiocarbamazone
lcsh:QD241-441
lcsh:Organic chemistry
antifungal agent
thiosemicarbazone derivative
conference paper
mass spectrometry
heterocyclic compound
chemistry.chemical_classification
Antiinfective agent
3
4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3'
4' dimethoxyphenyl) 2 phenyl 1
3
4 thiadiazoline
4
4' dimethoxybenzophenone thiocarbamazone
Organic Chemistry
spiro[5 acetamido 3 n acetyl 2
1' (6' methoxyindan)] 1
3
4 thiadiazoline
ketone derivative
spiro[5 acetamido 3 n acetyl 2
1' (1'
2'
3'
4' tetrahydronaphthalen)] 1
3
4 thiadiazoline
carbon nuclear magnetic resonance
Combinatorial chemistry
5 acetamido 3 n acetyl 2
2 diphenyl 1
3 thiadiazoline
unclassified drug
Characterization (materials science)
anthrone thiosemicarbazone
antiinfective agent
chemistry
Heterocyclic compound
hydrogen
3
4 dihydronaphthalen 1(2h) one thiosemicarbazone
5 acetamido 3 n acetyl 2
2 bis(4' methoxyphenyl) 1
3
4 thiadiazoline
indan 1 one thiosemicarbazone
chemical structure
Proton NMR
drug synthesis
thiadiazole derivative
spiro[5 acetamido 3 n acetyl 2
1' indane] 1
3
4 thiadiazoline
Zdroj: ARKIVOC, Vol 2000, Iss 4, Pp 627-640 (2000)
Scopus-Elsevier
Arkivoc 2000;2000(4 SPECISS):627-640
Biblioteca Digital (UBA-FCEN)
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
ISSN: 1551-7012
1551-7004
Popis: The synthesis of new 1,3,4-thiadiazolines derived from diaryl and aryl-cycloalkyl ketones, via the corresponding thiosemicarbazones, is described. Hand C-NMR spectra as well as mass spectrometry disclosed the structures of the precursors and heterocyclic derivatives formed. In the case of spirane compounds, the effect of heteroatoms (S, N) on the diastereotopic hydrogens is discussed.
Databáze: OpenAIRE
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