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

Organic & Biomolecular Chemistry · 2008 · Vol. 6(8) · pp. 1317–1317
Takanori ShibataKyoji Tsuchikama

Abstract

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.

Axial and Atropisomeric Chirality SynthesisCatalytic C–H Functionalization MethodsCatalytic Alkyne ReactionsEnantioselective synthesisAlkyneCycloadditionAlkeneChemistryRhodiumIntramolecular forceChirality (physics)MoietyCatalysis

Funding

  • Waseda University
Citations
300
FWCI
14.88
field-weighted impact
References
57
Percentile
100%
vs. same field & year
Citations per year
References
Transition Metal Catalyzed [2+2+2] Cycloaddition and Application in Organic Synthesis
European Journal of Organic Chemistry · 2005 · 499 citations
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