Synthesis and characterization of 2,2-disubstituted thiadiazolines

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:	Artículo publishedVersion
Publicado:	2000
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 https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai
Aporte de:	Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires

id	I28-R145-paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai
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spelling	I28-R145-paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai2024-08-16 Martins Alho, M.A. Moglioni, A.G. Brousse, B. Moltrasio, G.Y. D'Accorso, N.B. 2000 Fil:Martins Alho, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Moltrasio, G.Y. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. application/pdf http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Arkivoc 2000;2000(4 SPECISS):627-640 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 Synthesis and characterization of 2,2-disubstituted thiadiazolines info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-145
collection	Repositorio Digital de la Universidad de Buenos Aires (UBA)
topic	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
spellingShingle	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 Martins Alho, M.A. Moglioni, A.G. Brousse, B. Moltrasio, G.Y. D'Accorso, N.B. Synthesis and characterization of 2,2-disubstituted thiadiazolines
topic_facet	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
description	Fil:Martins Alho, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
format	Artículo Artículo publishedVersion
author	Martins Alho, M.A. Moglioni, A.G. Brousse, B. Moltrasio, G.Y. D'Accorso, N.B.
author_facet	Martins Alho, M.A. Moglioni, A.G. Brousse, B. Moltrasio, G.Y. D'Accorso, N.B.
author_sort	Martins Alho, M.A.
title	Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_short	Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_full	Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_fullStr	Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_full_unstemmed	Synthesis and characterization of 2,2-disubstituted thiadiazolines
title_sort	synthesis and characterization of 2,2-disubstituted thiadiazolines
publishDate	2000
url	http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai
work_keys_str_mv	AT martinsalhoma synthesisandcharacterizationof22disubstitutedthiadiazolines AT moglioniag synthesisandcharacterizationof22disubstitutedthiadiazolines AT brousseb synthesisandcharacterizationof22disubstitutedthiadiazolines AT moltrasiogy synthesisandcharacterizationof22disubstitutedthiadiazolines AT daccorsonb synthesisandcharacterizationof22disubstitutedthiadiazolines
_version_	1809356834175188992

Synthesis and characterization of 2,2-disubstituted thiadiazolines

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