Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate

In the title compound, C(39)H(45)NO(7),the pyrrolidine ring is connected to an estrone group, a trimeth­oxy benzene and a phenyl ring. The pyrrolidine ring exhibits a twist conformation and the other five-membered ring an envelope conformation. Mol­ecules are linked by N—H⋯O hydrogen bonds, C—H⋯π in...

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Autores principales: Kamala, E. Theboral Sugi, Murugan, R., Nirmala, S., Sudha, L., Narayanan, S. Sriman
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959683/
https://www.ncbi.nlm.nih.gov/pubmed/21581075
http://dx.doi.org/10.1107/S1600536808034582
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author Kamala, E. Theboral Sugi
Murugan, R.
Nirmala, S.
Sudha, L.
Narayanan, S. Sriman
author_facet Kamala, E. Theboral Sugi
Murugan, R.
Nirmala, S.
Sudha, L.
Narayanan, S. Sriman
author_sort Kamala, E. Theboral Sugi
collection PubMed
description In the title compound, C(39)H(45)NO(7),the pyrrolidine ring is connected to an estrone group, a trimeth­oxy benzene and a phenyl ring. The pyrrolidine ring exhibits a twist conformation and the other five-membered ring an envelope conformation. Mol­ecules are linked by N—H⋯O hydrogen bonds, C—H⋯π inter­actions and C—H⋯O hydrogen bonds.
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spelling pubmed-29596832010-12-30 Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate Kamala, E. Theboral Sugi Murugan, R. Nirmala, S. Sudha, L. Narayanan, S. Sriman Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(39)H(45)NO(7),the pyrrolidine ring is connected to an estrone group, a trimeth­oxy benzene and a phenyl ring. The pyrrolidine ring exhibits a twist conformation and the other five-membered ring an envelope conformation. Mol­ecules are linked by N—H⋯O hydrogen bonds, C—H⋯π inter­actions and C—H⋯O hydrogen bonds. International Union of Crystallography 2008-10-31 /pmc/articles/PMC2959683/ /pubmed/21581075 http://dx.doi.org/10.1107/S1600536808034582 Text en © Kamala et al. 2008 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
Kamala, E. Theboral Sugi
Murugan, R.
Nirmala, S.
Sudha, L.
Narayanan, S. Sriman
Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title_full Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title_fullStr Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title_full_unstemmed Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title_short Ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
title_sort ethyl 3-hydr­oxy-13-methyl-4′-phenyl-2′-(3,4,5-trimethoxy­phen­yl)-6,7,8,9,11,12,13,14,15,16-deca­hydro­spiro­[cyclo­penta­[a]phenanthrene-16,3′-pyrrolidine]-5′-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959683/
https://www.ncbi.nlm.nih.gov/pubmed/21581075
http://dx.doi.org/10.1107/S1600536808034582
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