4.6 Article

Recent advances in enantioselective [2+2+2] cycloaddition

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 6, Issue 8, Pages 1317-1323

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b720031e

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Enantioselective cycloaddition using chiral transition metal catalysts is an atom-economical and efficient synthetic tool for the construction of chiral carbo- and heterocyclic skeletons. This short account discloses our recent results of inter- and intramolecular enantioselective [2 + 2 + 2] cycloadditions of alkyne and/or alkene moiety(ies). Chiral iridium complexes catalyzed the alkyne trimerization for the generation of axial chirality(ies), and chiral rhodium ones catalyzed alkyne-alkyne-alkene cyclization for the generation of a quaternary carbon including spirocyclic system.

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