6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene

The title compound, C(76)H(80)O(16), is a macrocyclic structure. This novel resorcin[4]arene derivative has (meth­oxy­carbon­yl)meth­oxy ‘head’ groups on the upper rim. The compound has a C (2v) ‘boat’ geometry and there are a range of C—H⋯O contacts in the crystal structure.

Detalles Bibliográficos
Autores principales: Pansuriya, Pramod B., Friedrich, Holger B., Maguire, Glenn E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254447/
https://www.ncbi.nlm.nih.gov/pubmed/22259595
http://dx.doi.org/10.1107/S1600536811051567
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author Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
author_facet Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
author_sort Pansuriya, Pramod B.
collection PubMed
description The title compound, C(76)H(80)O(16), is a macrocyclic structure. This novel resorcin[4]arene derivative has (meth­oxy­carbon­yl)meth­oxy ‘head’ groups on the upper rim. The compound has a C (2v) ‘boat’ geometry and there are a range of C—H⋯O contacts in the crystal structure.
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spelling pubmed-32544472012-01-18 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene Pansuriya, Pramod B. Friedrich, Holger B. Maguire, Glenn E. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(76)H(80)O(16), is a macrocyclic structure. This novel resorcin[4]arene derivative has (meth­oxy­carbon­yl)meth­oxy ‘head’ groups on the upper rim. The compound has a C (2v) ‘boat’ geometry and there are a range of C—H⋯O contacts in the crystal structure. International Union of Crystallography 2011-12-10 /pmc/articles/PMC3254447/ /pubmed/22259595 http://dx.doi.org/10.1107/S1600536811051567 Text en © Pansuriya et al. 2012 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
Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title_full 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title_fullStr 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title_full_unstemmed 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title_short 6,12,18,24-Tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
title_sort 6,12,18,24-tetra­meth­oxy-4,10,16,22-tetra­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­kis­(2-phenyl­eth­yl)resorcin[4]arene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254447/
https://www.ncbi.nlm.nih.gov/pubmed/22259595
http://dx.doi.org/10.1107/S1600536811051567
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AT maguireglennem 6121824tetramethoxy4101622tetrakismethoxycarbonylmethoxy281420tetrakis2phenylethylresorcin4arene

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