Cargando…

[2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron

The title compound, C(13)H(18)BNO(4), was readily obtained from the reaction of methyl 4-boronobenzene acetate with ethano­lamine. A combination of inter­molecular N—H⋯O hydrogen bonds and C—H⋯π inter­actions leads to the pairwise association of mol­ecules.

Detalles Bibliográficos
Autores principales: Zein, Ahmed L., Dawe, Louise N., Georghiou, Paris E.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983237/
https://www.ncbi.nlm.nih.gov/pubmed/21587617
http://dx.doi.org/10.1107/S1600536810037864
_version_ 1782191833381601280
author Zein, Ahmed L.
Dawe, Louise N.
Georghiou, Paris E.
author_facet Zein, Ahmed L.
Dawe, Louise N.
Georghiou, Paris E.
author_sort Zein, Ahmed L.
collection PubMed
description The title compound, C(13)H(18)BNO(4), was readily obtained from the reaction of methyl 4-boronobenzene acetate with ethano­lamine. A combination of inter­molecular N—H⋯O hydrogen bonds and C—H⋯π inter­actions leads to the pairwise association of mol­ecules.
format Text
id pubmed-2983237
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29832372010-12-30 [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron Zein, Ahmed L. Dawe, Louise N. Georghiou, Paris E. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(18)BNO(4), was readily obtained from the reaction of methyl 4-boronobenzene acetate with ethano­lamine. A combination of inter­molecular N—H⋯O hydrogen bonds and C—H⋯π inter­actions leads to the pairwise association of mol­ecules. International Union of Crystallography 2010-09-30 /pmc/articles/PMC2983237/ /pubmed/21587617 http://dx.doi.org/10.1107/S1600536810037864 Text en © Zein 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
Zein, Ahmed L.
Dawe, Louise N.
Georghiou, Paris E.
[2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title_full [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title_fullStr [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title_full_unstemmed [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title_short [2,2′-Imino­diethano­lato(2−)-κ(3) O,N,O′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
title_sort [2,2′-imino­diethano­lato(2−)-κ(3) o,n,o′][4-(meth­oxy­carbonyl­meth­yl)phen­yl]boron
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983237/
https://www.ncbi.nlm.nih.gov/pubmed/21587617
http://dx.doi.org/10.1107/S1600536810037864
work_keys_str_mv AT zeinahmedl 22iminodiethanolato2k3ono4methoxycarbonylmethylphenylboron
AT dawelouisen 22iminodiethanolato2k3ono4methoxycarbonylmethylphenylboron
AT georghiouparise 22iminodiethanolato2k3ono4methoxycarbonylmethylphenylboron