المؤلفون: Martins Alho, M.A., Moglioni, A.G., Brousse, B., Moltrasio, G.Y., D'Accorso, N.B.

المصدر: Arkivoc 2000;2000(4 SPECISS):627-640

مصطلحات موضوعية: 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)], spiro[5 acetamido 3 n acetyl 2,1' (6' methoxyindan)], spiro[5 acetamido 3 n acetyl 2,1' indane], thiadiazole derivative, thiosemicarbazone derivative, unclassified drug, carbon nuclear magnetic resonance, chemical structure, conference paper, drug synthesis, mass spectrometry

وصف الملف: application/pdf

Relation: http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho; http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai

الاتاحة: https://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2000_n4SPECISS_p627_MartinsAlho_oai

المؤلفون: M. A. Martins Alho, Beatriz N. Brousse, Albertina G. Moglioni, Norma D´Accorso, Graciela Y. Moltrasio

المصدر: 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

مصطلحات موضوعية: 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

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7347c3859ba0ae4db3b74d756a439f6
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0001.413

المؤلفون: Martins Alho, M.A., Moglioni, A.G., Brousse, B., Moltrasio, G.Y., D'Accorso, N.B.

مصطلحات موضوعية: 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

Relation: http://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho

الاتاحة: https://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho

المؤلفون: Martins Alho, Miriam Amelia, Moltrasio, Graciela Yolanda, D'Accorso, Norma Beatriz

مصطلحات موضوعية: 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

Relation: 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

الاتاحة: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho
https://hdl.handle.net/20.500.12110/paper_14246376_v2000_n4SPECISS_p627_MartinsAlho