1′-Ethyl-sulfanyl-1,1′-bicyclo-hexyl-2-one

Lalit Kumar Sharma; Sean Parkin; Gregory I. Elliott

doi:10.1107/S1600536810010731

1′-Ethyl-sulfanyl-1,1′-bicyclo-hexyl-2-one

Lalit Kumar Sharma, Sean Parkin, Gregory I. Elliott

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

There are two independent molecules in the asymmetric unit of the title cyclo-hexa-none derivative, C₁₄H₂₄OS, in which both cyclo-hexane rings exhibit chair conformations. They are also equatorial to each other, which permits the ethanethiol substituent to be in a syn conformation with the -H atom of the parent attached cyclo-hexa-none.

Original language	English
Pages (from-to)	o932
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	66
Issue number	4
DOIs	https://doi.org/10.1107/S1600536810010731
State	Published - 2010

ASJC Scopus subject areas

Chemistry (all)
Materials Science (all)
Condensed Matter Physics

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title = "1′-Ethyl-sulfanyl-1,1′-bicyclo-hexyl-2-one",

abstract = "There are two independent molecules in the asymmetric unit of the title cyclo-hexa-none derivative, C14H24OS, in which both cyclo-hexane rings exhibit chair conformations. They are also equatorial to each other, which permits the ethanethiol substituent to be in a syn conformation with the -H atom of the parent attached cyclo-hexa-none.",

author = "Sharma, {Lalit Kumar} and Sean Parkin and Elliott, {Gregory I.}",

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language = "English",

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AU - Sharma, Lalit Kumar

AU - Parkin, Sean

AU - Elliott, Gregory I.

PY - 2010

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N2 - There are two independent molecules in the asymmetric unit of the title cyclo-hexa-none derivative, C14H24OS, in which both cyclo-hexane rings exhibit chair conformations. They are also equatorial to each other, which permits the ethanethiol substituent to be in a syn conformation with the -H atom of the parent attached cyclo-hexa-none.

AB - There are two independent molecules in the asymmetric unit of the title cyclo-hexa-none derivative, C14H24OS, in which both cyclo-hexane rings exhibit chair conformations. They are also equatorial to each other, which permits the ethanethiol substituent to be in a syn conformation with the -H atom of the parent attached cyclo-hexa-none.

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1′-Ethyl-sulfanyl-1,1′-bicyclo-hexyl-2-one

Abstract

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