Publication | Closed Access
Evolution of Efficient Strategies for Enone−Alkyne and Enal−Alkyne Reductive Couplings
71
Citations
49
References
2009
Year
Asymmetric CatalysisCross-coupling ReactionEngineeringPhysicsEfficient StrategiesNatural SciencesApplied PhysicsExcitation Energy TransferOrganic ChemistryStereoselective SynthesisChemistryQuantum ChemistryReductive CouplingMechanistic ProposalsMany Functional GroupsEnantioselective SynthesisBiomolecular Engineering
Strategies for the reductive coupling of enones or enals with alkynes have been developed. The reducing agents employed include organozincs, organoboranes, organosilanes, and methanol. The latter of these strategies is simple, cost-effective, and tolerant of many functional groups. Isotopic labeling strategies have provided supporting evidence for the mechanistic proposals.
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