Exploitation of Rh(I)-Rh(III) cycles in enantioselective C-C bond cleavages: access to beta-tetralones and benzobicyclo[2.2.2]octanones

Souillart, LaetitiaCramer, Nicolai2014-02-172014-02-172014-02-17201410.1039/c3sc52753khttps://infoscience.epfl.ch/handle/20.500.14299/100756WOS:000328954200051Rhodium(I)-catalyzed beta-carbon eliminations of tert-cyclobutanols followed by oxidative addition give benzorhoda(III)cyclopentenes. These key intermediates trigger intramolecular C-H arylations leading to beta-tetralones with quaternary stereogenic centers in excellent enantioselectivity. The versatility of the rhoda(III)cyclic species is further shown in formal intramolecular [4+2]-cycloadditions providing access to benzobicyclo[2.2.2]octanones.Exploitation of Rh(I)-Rh(III) cycles in enantioselective C-C bond cleavages: access to beta-tetralones and benzobicyclo[2.2.2]octanonestext::journal::journal article::research article