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Clathrates of TETROL: selective inclusion of methylcyclohexanones in their energetically unfavorable axial methyl conformations†
B. Barton,M. R. Caira,E. C. Hosten,C. W. McCleland,S. Weitz
Chemical Communications Pub Date : 09/18/2014 00:00:00 , DOI:10.1039/C4CC06826B
Abstract

3- and 4-Methylcyclohexanone have been isolated exclusively as their energetically disfavoured axial conformers in the host–guest complexes formed upon recrystallization of the novel optically pure host compound, (+)-(2R,3R)-1,1,4,4-tetraphenylbutane-1,2,3,4-tetraol (TETROL), from these cycloalkanones.

Graphical abstract: Clathrates of TETROL: selective inclusion of methylcyclohexanones in their energetically unfavorable axial methyl conformations
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