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Title: Catalytic alkene cyclohydroamination via an imido mechanism. Author: Gott AL, Clarke AJ, Clarkson GJ, Scott P. Journal: Chem Commun (Camb); 2008 Mar 28; (12):1422-4. PubMed ID: 18338043. Abstract: Chiral-at-metal half-sandwich diamide complexes catalyse enantioselective cyclohydroamination of aminoalkenes at unexpectedly high rates given their high coordination number and steric bulk; substantial evidence is presented which argues against the established sigma-bond insertion process and is strongly indicative of an imido [2+2] cycloaddition mechanism.[Abstract] [Full Text] [Related] [New Search]