tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate

In the title compound, C(19)H(24)O(4), the six-membered lactone ring adopts an envelope conformation with the tert-butoxy­carbonyl and isopropyl substituents in axial positions, and the phenyl group in an equatorial position. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link t...

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Detalles Bibliográficos
Autores principales: Chen, Wei, Yu, Miao, Li, Si, Jiao, Ning
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979271/
https://www.ncbi.nlm.nih.gov/pubmed/21579155
http://dx.doi.org/10.1107/S160053681001367X
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author Chen, Wei
Yu, Miao
Li, Si
Jiao, Ning
author_facet Chen, Wei
Yu, Miao
Li, Si
Jiao, Ning
author_sort Chen, Wei
collection PubMed
description In the title compound, C(19)H(24)O(4), the six-membered lactone ring adopts an envelope conformation with the tert-butoxy­carbonyl and isopropyl substituents in axial positions, and the phenyl group in an equatorial position. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers.
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spelling pubmed-29792712010-12-30 tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate Chen, Wei Yu, Miao Li, Si Jiao, Ning Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(24)O(4), the six-membered lactone ring adopts an envelope conformation with the tert-butoxy­carbonyl and isopropyl substituents in axial positions, and the phenyl group in an equatorial position. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. International Union of Crystallography 2010-04-17 /pmc/articles/PMC2979271/ /pubmed/21579155 http://dx.doi.org/10.1107/S160053681001367X Text en © Chen et al. 2010 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
Chen, Wei
Yu, Miao
Li, Si
Jiao, Ning
tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title_full tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title_fullStr tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title_full_unstemmed tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title_short tert-Butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2H-pyran-3-carboxyl­ate
title_sort tert-butyl 4-isopropyl-2-oxo-6-phenyl-3,4-dihydro-2h-pyran-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979271/
https://www.ncbi.nlm.nih.gov/pubmed/21579155
http://dx.doi.org/10.1107/S160053681001367X
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