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

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
Publicado: 1998
Materias:
13C NMR
1H NMR
Benzo[a]phenazines
NMR
β-lapachone
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v36_n7_p529_BenedettiDoctorovich
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 paper:paper_07491581_v36_n7_p529_BenedettiDoctorovich
record_format dspace
spelling paper:paper_07491581_v36_n7_p529_BenedettiDoctorovich2023-06-08T15:45:32Z Preparation and NMR characterization of new substituted benzo[a]phenazines 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. 1998 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v36_n7_p529_BenedettiDoctorovich 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
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.
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
publishDate 1998
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v36_n7_p529_BenedettiDoctorovich
http://hdl.handle.net/20.500.12110/paper_07491581_v36_n7_p529_BenedettiDoctorovich
_version_ 1768543328792477696

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