Cargando…

(1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate

In the title compound C(26)H(25)NO(7), the mean plane through the lactone-substituted ring of the pyrrolizidine moiety forms dihedral angles of 78.46 (6) and 58.28 (8)° with the ace­naphthyl­ene moiety and the sugar based-lactone ring, respectively. The sum of the angles at the the N atom of the pyr...

Descripción completa

Detalles Bibliográficos
Autores principales: Santhiya, S., Naga Siva Rao, J., Raghunathan, R., Latha, N., Lakshmi, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884278/
https://www.ncbi.nlm.nih.gov/pubmed/24454054
http://dx.doi.org/10.1107/S1600536813026111
_version_ 1782298553843974144
author Santhiya, S.
Naga Siva Rao, J.
Raghunathan, R.
Latha, N.
Lakshmi, S.
author_facet Santhiya, S.
Naga Siva Rao, J.
Raghunathan, R.
Latha, N.
Lakshmi, S.
author_sort Santhiya, S.
collection PubMed
description In the title compound C(26)H(25)NO(7), the mean plane through the lactone-substituted ring of the pyrrolizidine moiety forms dihedral angles of 78.46 (6) and 58.28 (8)° with the ace­naphthyl­ene moiety and the sugar based-lactone ring, respectively. The sum of the angles at the the N atom of the pyrrolizidine ring (335.0°) is in accordance with sp (3) hybridization. Some atoms of the acetate group are disordered and were refined using a split model [occupancy ratio 0.673 (10):0.327 (10)].
format Online
Article
Text
id pubmed-3884278
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-38842782014-01-17 (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate Santhiya, S. Naga Siva Rao, J. Raghunathan, R. Latha, N. Lakshmi, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound C(26)H(25)NO(7), the mean plane through the lactone-substituted ring of the pyrrolizidine moiety forms dihedral angles of 78.46 (6) and 58.28 (8)° with the ace­naphthyl­ene moiety and the sugar based-lactone ring, respectively. The sum of the angles at the the N atom of the pyrrolizidine ring (335.0°) is in accordance with sp (3) hybridization. Some atoms of the acetate group are disordered and were refined using a split model [occupancy ratio 0.673 (10):0.327 (10)]. International Union of Crystallography 2013-10-02 /pmc/articles/PMC3884278/ /pubmed/24454054 http://dx.doi.org/10.1107/S1600536813026111 Text en © Santhiya et al. 2013 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
Santhiya, S.
Naga Siva Rao, J.
Raghunathan, R.
Latha, N.
Lakshmi, S.
(1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title_full (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title_fullStr (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title_full_unstemmed (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title_short (1S,1′S,2′R,4a’S,9a’S,9b’R)-1′-Acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′H,2H-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
title_sort (1s,1′s,2′r,4a’s,9a’s,9b’r)-1′-acet­yloxy-2,4′-dioxo-2′,4′,4a’,7′,8′,9′,9a’,9b’-octa­hydro-1′h,2h-spiro­[ace­naphthyl­ene-1,5′-pyrano[4,3-a]pyrrolizin]-2′-ylmethyl acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884278/
https://www.ncbi.nlm.nih.gov/pubmed/24454054
http://dx.doi.org/10.1107/S1600536813026111
work_keys_str_mv AT santhiyas 1s1s2r4as9as9br1acetyloxy24dioxo244a7899a9boctahydro1h2hspiroacenaphthylene15pyrano43apyrrolizin2ylmethylacetate
AT nagasivaraoj 1s1s2r4as9as9br1acetyloxy24dioxo244a7899a9boctahydro1h2hspiroacenaphthylene15pyrano43apyrrolizin2ylmethylacetate
AT raghunathanr 1s1s2r4as9as9br1acetyloxy24dioxo244a7899a9boctahydro1h2hspiroacenaphthylene15pyrano43apyrrolizin2ylmethylacetate
AT lathan 1s1s2r4as9as9br1acetyloxy24dioxo244a7899a9boctahydro1h2hspiroacenaphthylene15pyrano43apyrrolizin2ylmethylacetate
AT lakshmis 1s1s2r4as9as9br1acetyloxy24dioxo244a7899a9boctahydro1h2hspiroacenaphthylene15pyrano43apyrrolizin2ylmethylacetate