Publication | Closed Access
Direct Vicinal Difunctionalization of Alkynes: An Efficient Approach Towards the Synthesis of Highly Functionalized Fluorinated Alkenes
132
Citations
136
References
2015
Year
Chemical EngineeringCross-coupling ReactionDerivativesDirect Vicinal DifunctionalizationEngineeringAlkene MetathesisNatural SciencesDiversity-oriented SynthesisFluorous SynthesisEfficient ApproachOrganic ChemistryOrganometallic CatalysisCatalysisChemistrySynthesis MethodVersatile AlkynesBiomolecular EngineeringFunctional Group
Abstract The direct vicinal difunctionalization of versatile alkynes is an area of considerable interest. In particular, the concomitant introduction of a functional group and a fluorinated moiety offers new efficient synthetic routes to the construction of highly functionalized olefins, key building blocks in the synthesis of several complex and relevant molecules. This review highlights the major progress that has been made in this field offering an overview of the direct concomitant introduction of a range of functional groups and various fluorinated moieties into alkynes through radical and metal‐catalyzed processes. In addition, rearrangement reactions involving molecules containing alkynes and leading to fluorinated alkenes are also carefully depicted.
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