Cargando…

8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline

The title compound, C(18)H(19)NO, was synthesized from the multi-component one-pot reaction between p-toluidine, benzaldehyde and 2,3-dihydro­furan in the presence of palladium dichloride. There are two mol­ecules in the asymmetric unit. The crystal packing is stabilized by classical inter­molecular...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Pingping, Lian, Chaomei, Zhu, Yulin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980039/
https://www.ncbi.nlm.nih.gov/pubmed/21580056
http://dx.doi.org/10.1107/S1600536809051125
_version_ 1782191562835361792
author Lu, Pingping
Lian, Chaomei
Zhu, Yulin
author_facet Lu, Pingping
Lian, Chaomei
Zhu, Yulin
author_sort Lu, Pingping
collection PubMed
description The title compound, C(18)H(19)NO, was synthesized from the multi-component one-pot reaction between p-toluidine, benzaldehyde and 2,3-dihydro­furan in the presence of palladium dichloride. There are two mol­ecules in the asymmetric unit. The crystal packing is stabilized by classical inter­molecular N—H⋯O hydrogen bonds.
format Text
id pubmed-2980039
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29800392010-12-30 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline Lu, Pingping Lian, Chaomei Zhu, Yulin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(19)NO, was synthesized from the multi-component one-pot reaction between p-toluidine, benzaldehyde and 2,3-dihydro­furan in the presence of palladium dichloride. There are two mol­ecules in the asymmetric unit. The crystal packing is stabilized by classical inter­molecular N—H⋯O hydrogen bonds. International Union of Crystallography 2009-12-04 /pmc/articles/PMC2980039/ /pubmed/21580056 http://dx.doi.org/10.1107/S1600536809051125 Text en © Lu et al. 2010 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Lu, Pingping
Lian, Chaomei
Zhu, Yulin
8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title_full 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title_fullStr 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title_full_unstemmed 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title_short 8-Methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
title_sort 8-methyl-4-phenyl-2,3,3a,4,5,9b-hexa­hydro­furo[3,2-c]quinoline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980039/
https://www.ncbi.nlm.nih.gov/pubmed/21580056
http://dx.doi.org/10.1107/S1600536809051125
work_keys_str_mv AT lupingping 8methyl4phenyl233a459bhexahydrofuro32cquinoline
AT lianchaomei 8methyl4phenyl233a459bhexahydrofuro32cquinoline
AT zhuyulin 8methyl4phenyl233a459bhexahydrofuro32cquinoline