Synthesis and characterization of 2,2-disubstituted thiadiazolines

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Fil:Martins Alho, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.

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Detalles Bibliográficos
Autores principales: Martins Alho, M.A., Moglioni, A.G., Brousse, B., Moltrasio, G.Y., D'Accorso, N.B.
Formato: JOUR
Materias:
3,4 dihydronaphthalen 1(2h) one thiosemicarbazone
3,4' dimethoxybenzophenone thiocarbamazone
4 methoxybenzophenone thiocarbamazone
4,4' dimethoxybenzophenone thiocarbamazone
5 acetamido 3 n acetyl 2 (3',4' dimethoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2 (4' methoxyphenyl) 2 phenyl 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 bis(4' methoxyphenyl) 1,3,4 thiadiazoline
5 acetamido 3 n acetyl 2,2 diphenyl 1,3 thiadiazoline
5 methoxyindan 1 one thiosemicarbazone
6 methoxyindan 1 one thiosemicarbazone
anthrone thiosemicarbazone
antifungal agent
antiinfective agent
heterocyclic compound
hydrogen
indan 1 one thiosemicarbazone
ketone derivative
spiro[5 acetamido 3 n acetyl 2,1' (1',2',3',4' tetrahydronaphthalen)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (5' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)] 1,3,4 thiadiazoline
spiro[5 acetamido 3 n acetyl 2,1' indane] 1,3,4 thiadiazoline
thiadiazole derivative
thiosemicarbazone derivative
unclassified drug
carbon nuclear magnetic resonance
chemical structure
conference paper
drug synthesis
mass spectrometry
proton nuclear magnetic resonance
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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