Cargando…
1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate
In the title compound, C(27)H(20)NO(3)P, the P atom exhibits a somewhat distorted PNO(3) tetrahedral geometry, with the O—P—O angle for the binaphthyl fragment being 102.82 (6)°. The dihedral angle between the naphthyl ring systems is 59.00 (2)°. In the crystal, inversion dimers linked by pairs of...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238962/ https://www.ncbi.nlm.nih.gov/pubmed/22199811 http://dx.doi.org/10.1107/S1600536811046861 |
_version_ | 1782219093357625344 |
---|---|
author | Gowda, Ravikumar R Ramkumar, Venkatachalam Chakraborty, Debashis |
author_facet | Gowda, Ravikumar R Ramkumar, Venkatachalam Chakraborty, Debashis |
author_sort | Gowda, Ravikumar R |
collection | PubMed |
description | In the title compound, C(27)H(20)NO(3)P, the P atom exhibits a somewhat distorted PNO(3) tetrahedral geometry, with the O—P—O angle for the binaphthyl fragment being 102.82 (6)°. The dihedral angle between the naphthyl ring systems is 59.00 (2)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops. |
format | Online Article Text |
id | pubmed-3238962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32389622011-12-23 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate Gowda, Ravikumar R Ramkumar, Venkatachalam Chakraborty, Debashis Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(20)NO(3)P, the P atom exhibits a somewhat distorted PNO(3) tetrahedral geometry, with the O—P—O angle for the binaphthyl fragment being 102.82 (6)°. The dihedral angle between the naphthyl ring systems is 59.00 (2)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2011-11-16 /pmc/articles/PMC3238962/ /pubmed/22199811 http://dx.doi.org/10.1107/S1600536811046861 Text en © Gowda et al. 2011 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 Gowda, Ravikumar R Ramkumar, Venkatachalam Chakraborty, Debashis 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title | 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title_full | 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title_fullStr | 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title_full_unstemmed | 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title_short | 1,1′-Binaphthyl-2,2′-diyl benzylphosphoramidate |
title_sort | 1,1′-binaphthyl-2,2′-diyl benzylphosphoramidate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238962/ https://www.ncbi.nlm.nih.gov/pubmed/22199811 http://dx.doi.org/10.1107/S1600536811046861 |
work_keys_str_mv | AT gowdaravikumarr 11binaphthyl22diylbenzylphosphoramidate AT ramkumarvenkatachalam 11binaphthyl22diylbenzylphosphoramidate AT chakrabortydebashis 11binaphthyl22diylbenzylphosphoramidate |