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The enantioselective intramolecular aminative functionalization of unactivated alkenes, dienes, allenes and alkynes for the synthesis of chiral nitrogen heterocycles

Organic & Biomolecular Chemistry · 2009 · Vol. 7(15) · pp. 3009–3009
Sherry R. Chemler

Abstract

The enantioselective intramolecular aminative functionalization of unactivated alkenes and related π-systems is a straight-forward and atom economical strategy for the synthesis of chiral nitrogen heterocycles. These reactions can be categorized as oxidatively neutral, such as alkene hydroamination, or as oxidative reactions, such as alkene difunctionalization, e.g. aminooxygenation and carboamination. This perspective reviews the current work in the field and explores mechanistic trends that are common among the different catalysts and reaction types.

Catalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsAsymmetric Synthesis and CatalysisHydroaminationEnantioselective synthesisChemistryAlkeneIntramolecular forceSurface modificationCatalysisAminationNitrogen atomCombinatorial chemistry

Funding

  • National Institutes of Health
Citations
274
FWCI
14.56
field-weighted impact
References
49
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99%
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Cited by
Recent Advances in Radical Difunctionalization of Simple Alkenes
European Journal of Organic Chemistry · 2017 · 473 citations
References
Gold‐Catalyzed Hydroamination of C–C Multiple Bonds
European Journal of Organic Chemistry · 2006 · 501 citations
Recent Developments in Enantioselective Gold(I) Catalysis
Chemistry - A European Journal · 2008 · 565 citations
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Gold‐Catalyzed Hydroamination of C–C Multiple Bonds
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