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:	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

id	todo:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
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spelling	todo:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho2023-10-03T16:13:36Z Synthesis and characterization of 2,2-disubstituted thiadiazolines Martins Alho, M.A. Moglioni, A.G. Brousse, B. Moltrasio, G.Y. D'Accorso, N.B. 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 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-134
collection	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (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	JOUR
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
url	http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
work_keys_str_mv	AT martinsalhoma synthesisandcharacterizationof22disubstitutedthiadiazolines AT moglioniag synthesisandcharacterizationof22disubstitutedthiadiazolines AT brousseb synthesisandcharacterizationof22disubstitutedthiadiazolines AT moltrasiogy synthesisandcharacterizationof22disubstitutedthiadiazolines AT daccorsonb synthesisandcharacterizationof22disubstitutedthiadiazolines
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Synthesis and characterization of 2,2-disubstituted thiadiazolines

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