Preparation and NMR characterization of new substituted benzo[a]phenazines

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Benzo[a]phenazines were prepared by condensation of β-lapachone with 1,2-phenylenediamme and 4-chloro-1,2-phenylenediamine. The latter diamine gave two regioisomers that could be separated and unambiguously identified by means of their 1H and 13C NMR spectra with the aid of 2D NMR experiments, mainl...

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Detalles Bibliográficos
Autores principales: Benedetti-Doctorovich, V., Escola, N., Burton, G.
Formato: JOUR
Materias:
13C NMR
1H NMR
Benzo[a]phenazines
NMR
β-lapachone
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_07491581_v36_n7_p529_BenedettiDoctorovich
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id todo:paper_07491581_v36_n7_p529_BenedettiDoctorovich
record_format dspace
spelling todo:paper_07491581_v36_n7_p529_BenedettiDoctorovich2023-10-03T15:39:24Z Preparation and NMR characterization of new substituted benzo[a]phenazines Benedetti-Doctorovich, V. Escola, N. Burton, G. 13C NMR 1H NMR Benzo[a]phenazines NMR β-lapachone Benzo[a]phenazines were prepared by condensation of β-lapachone with 1,2-phenylenediamme and 4-chloro-1,2-phenylenediamine. The latter diamine gave two regioisomers that could be separated and unambiguously identified by means of their 1H and 13C NMR spectra with the aid of 2D NMR experiments, mainly HETCOR and COLOC. © 1998 John Wiley & Sons, Ltd. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_07491581_v36_n7_p529_BenedettiDoctorovich
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 13C NMR
1H NMR
Benzo[a]phenazines
NMR
β-lapachone
spellingShingle 13C NMR
1H NMR
Benzo[a]phenazines
NMR
β-lapachone
Benedetti-Doctorovich, V.
Escola, N.
Burton, G.
Preparation and NMR characterization of new substituted benzo[a]phenazines
topic_facet 13C NMR
1H NMR
Benzo[a]phenazines
NMR
β-lapachone
description Benzo[a]phenazines were prepared by condensation of β-lapachone with 1,2-phenylenediamme and 4-chloro-1,2-phenylenediamine. The latter diamine gave two regioisomers that could be separated and unambiguously identified by means of their 1H and 13C NMR spectra with the aid of 2D NMR experiments, mainly HETCOR and COLOC. © 1998 John Wiley & Sons, Ltd.
format JOUR
author Benedetti-Doctorovich, V.
Escola, N.
Burton, G.
author_facet Benedetti-Doctorovich, V.
Escola, N.
Burton, G.
author_sort Benedetti-Doctorovich, V.
title Preparation and NMR characterization of new substituted benzo[a]phenazines
title_short Preparation and NMR characterization of new substituted benzo[a]phenazines
title_full Preparation and NMR characterization of new substituted benzo[a]phenazines
title_fullStr Preparation and NMR characterization of new substituted benzo[a]phenazines
title_full_unstemmed Preparation and NMR characterization of new substituted benzo[a]phenazines
title_sort preparation and nmr characterization of new substituted benzo[a]phenazines
url http://hdl.handle.net/20.500.12110/paper_07491581_v36_n7_p529_BenedettiDoctorovich
work_keys_str_mv AT benedettidoctorovichv preparationandnmrcharacterizationofnewsubstitutedbenzoaphenazines
AT escolan preparationandnmrcharacterizationofnewsubstitutedbenzoaphenazines
AT burtong preparationandnmrcharacterizationofnewsubstitutedbenzoaphenazines
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