Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate

The title compound, C(24)H(22)O(4)S, was prepared by reaction between (2E)-3-(6-meth­oxy-2-naphth­yl)-1-(2-thien­yl)prop-2-en-1-one and ethyl acetoacetate. In the crystal, the cyclo­hexenone ring shows a distorted half-chair conformation. The length of the double bond in the cyclohexenone ring [1.34...

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Detalles Bibliográficos
Autores principales: Li, Hongqi, Mayekar, Anil N., Narayana, B., Yathirajan, H. S., Harrison, W. T. A.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969391/
https://www.ncbi.nlm.nih.gov/pubmed/21582822
http://dx.doi.org/10.1107/S1600536809021308
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author Li, Hongqi
Mayekar, Anil N.
Narayana, B.
Yathirajan, H. S.
Harrison, W. T. A.
author_facet Li, Hongqi
Mayekar, Anil N.
Narayana, B.
Yathirajan, H. S.
Harrison, W. T. A.
author_sort Li, Hongqi
collection PubMed
description The title compound, C(24)H(22)O(4)S, was prepared by reaction between (2E)-3-(6-meth­oxy-2-naphth­yl)-1-(2-thien­yl)prop-2-en-1-one and ethyl acetoacetate. In the crystal, the cyclo­hexenone ring shows a distorted half-chair conformation. The length of the double bond in the cyclohexenone ring [1.343 (4) Å] is normal.
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spelling pubmed-29693912010-12-30 Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate Li, Hongqi Mayekar, Anil N. Narayana, B. Yathirajan, H. S. Harrison, W. T. A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(22)O(4)S, was prepared by reaction between (2E)-3-(6-meth­oxy-2-naphth­yl)-1-(2-thien­yl)prop-2-en-1-one and ethyl acetoacetate. In the crystal, the cyclo­hexenone ring shows a distorted half-chair conformation. The length of the double bond in the cyclohexenone ring [1.343 (4) Å] is normal. International Union of Crystallography 2009-06-10 /pmc/articles/PMC2969391/ /pubmed/21582822 http://dx.doi.org/10.1107/S1600536809021308 Text en © Li et al. 2009 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
Li, Hongqi
Mayekar, Anil N.
Narayana, B.
Yathirajan, H. S.
Harrison, W. T. A.
Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title_full Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title_fullStr Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title_full_unstemmed Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title_short Ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
title_sort ethyl 6-(6-meth­oxy-2-naphth­yl)-2-oxo-4-(2-thien­yl)cyclo­hex-3-ene-1-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969391/
https://www.ncbi.nlm.nih.gov/pubmed/21582822
http://dx.doi.org/10.1107/S1600536809021308
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AT narayanab ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
AT yathirajanhs ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
AT harrisonwta ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate

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