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, Miriam Amelia, Moltrasio, Graciela Yolanda, D'Accorso, Norma Beatriz
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:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho 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	paper:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
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spelling	paper:paper_14246376_v2000_n4SPECISS_p627_MartinsAlho2023-06-08T16:13:51Z Synthesis and characterization of 2,2-disubstituted thiadiazolines Martins Alho, Miriam Amelia Moltrasio, Graciela Yolanda D'Accorso, Norma Beatriz 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. 2000 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho 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, Miriam Amelia Moltrasio, Graciela Yolanda D'Accorso, Norma Beatriz 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.
author	Martins Alho, Miriam Amelia Moltrasio, Graciela Yolanda D'Accorso, Norma Beatriz
author_facet	Martins Alho, Miriam Amelia Moltrasio, Graciela Yolanda D'Accorso, Norma Beatriz
author_sort	Martins Alho, Miriam Amelia
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	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
work_keys_str_mv	AT martinsalhomiriamamelia synthesisandcharacterizationof22disubstitutedthiadiazolines AT moltrasiogracielayolanda synthesisandcharacterizationof22disubstitutedthiadiazolines AT daccorsonormabeatriz synthesisandcharacterizationof22disubstitutedthiadiazolines
_version_	1768543575431184384

Synthesis and characterization of 2,2-disubstituted thiadiazolines

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