Wipf, Peter Ribe, Seth Water-Accelerated Tandem Claisen Rearrangement−Catalytic Asymmetric Carboalumination The addition of stoichiometric quantities of water accelerates both the trimethylaluminum-mediated aromatic Claisen reaction and the chiral zirconocene-catalyzed asymmetric carboalumination of terminal alkenes. The two reactions occur in a tandem sequence resulting in the selective formation of two new C−C and one C−O bond after oxidative quench of the intermediate trialkylalane. carboalumination;trialkylalane;oxidative;terminal alkenes;Asymmetric;Tandem;bond;tandem sequence;formation;Rearrangement;stoichiometric quantities;chiral;Carboalumination;Claisen reaction;quantity 2001-04-14
    https://acs.figshare.com/articles/journal_contribution/Water-Accelerated_Tandem_Claisen_Rearrangement_Catalytic_Asymmetric_Carboalumination/3739026
10.1021/ol015816z.s001