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

The title compound, C24H22O4S, 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&...

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Main Authors: Hongqi Li, Anil N. Mayekar, B. Narayana, H. S. Yathirajan, W. T. A. Harrison
Format: Article
Language:English
Published: International Union of Crystallography 2009-07-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536809021308
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spelling doaj-bf00f41a1cf141449438319b33369e9f2020-11-25T00:59:44ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-07-01657o1533o153310.1107/S1600536809021308Ethyl 6-(6-methoxy-2-naphthyl)-2-oxo-4-(2-thienyl)cyclohex-3-ene-1-carboxylateHongqi LiAnil N. MayekarB. NarayanaH. S. YathirajanW. T. A. HarrisonThe title compound, C24H22O4S, 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. http://scripts.iucr.org/cgi-bin/paper?S1600536809021308
collection DOAJ
language English
format Article
sources DOAJ
author Hongqi Li
Anil N. Mayekar
B. Narayana
H. S. Yathirajan
W. T. A. Harrison
spellingShingle Hongqi Li
Anil N. Mayekar
B. Narayana
H. S. Yathirajan
W. T. A. Harrison
Ethyl 6-(6-methoxy-2-naphthyl)-2-oxo-4-(2-thienyl)cyclohex-3-ene-1-carboxylate
Acta Crystallographica Section E
author_facet Hongqi Li
Anil N. Mayekar
B. Narayana
H. S. Yathirajan
W. T. A. Harrison
author_sort Hongqi Li
title 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_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_sort ethyl 6-(6-methoxy-2-naphthyl)-2-oxo-4-(2-thienyl)cyclohex-3-ene-1-carboxylate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2009-07-01
description The title compound, C24H22O4S, 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.
url http://scripts.iucr.org/cgi-bin/paper?S1600536809021308
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AT anilnmayekar ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
AT bnarayana ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
AT hsyathirajan ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
AT wtaharrison ethyl66methoxy2naphthyl2oxo42thienylcyclohex3ene1carboxylate
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