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Review

Relative Stability of cis- and trans-Hydrindanones

Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-cho, Tokushima 770-8514, Japan
Academic Editor: Derek J. McPhee
Molecules 2015, 20(1), 1509-1518; https://doi.org/10.3390/molecules20011509
Received: 14 November 2014 / Accepted: 14 January 2015 / Published: 15 January 2015
(This article belongs to the Section Organic Chemistry)
The relative stabilities of several cis- and trans-hydrindanones were compared using both isomerization experiments and MM2 calculations. The generally believed rule that cis-hydrindanones are more stable than trans-isomers is applicable, but is not always true. This review introduces examples, mainly from studies in our laboratory, to explain these facts. View Full-Text
Keywords: hydrindanones; isomerization; isomer; stereochemistry; stability; MM2 hydrindanones; isomerization; isomer; stereochemistry; stability; MM2
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MDPI and ACS Style

Tori, M. Relative Stability of cis- and trans-Hydrindanones. Molecules 2015, 20, 1509-1518. https://doi.org/10.3390/molecules20011509

AMA Style

Tori M. Relative Stability of cis- and trans-Hydrindanones. Molecules. 2015; 20(1):1509-1518. https://doi.org/10.3390/molecules20011509

Chicago/Turabian Style

Tori, Motoo. 2015. "Relative Stability of cis- and trans-Hydrindanones" Molecules 20, no. 1: 1509-1518. https://doi.org/10.3390/molecules20011509

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