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- Chan-Lam_coupling abstract "The Chan–Lam coupling reaction – also known as the Chan–Evans–Lam coupling, as Chan, Evans, and Lam published their work back-to-back in Tetrahedron Letters – is a cross-coupling reaction between an aryl boronic acid and an alcohol or an amine to form the corresponding secondary aryl amines or aryl ethers, respectively. The Chan–Lam coupling is catalyzed in the presence of copper(II) species and may be conducted in air at room temperature. This is in contrast to the Buchwald–Hartwig coupling, which relies on the use of expensive noble metal catalysts (palladium), non-generalizable ligands, and a basic species (for deprotonation of the N-H and O-H bonds). In this regard, the Chan–Lam coupling has several benefits over other C-N and C-O coupling reactions. Because motifs containing aryl C-N and C-O bonds are frequently found in pharmaceuticals, the Chan–Lam coupling has seen a great deal of application. Often stoichiometric copper is used, as only a small amount of the copper proceeds to a catalytically active species. The mechanism, which is still rather controversial, is shown in the below figure:It is presently unknown whether the Chan-Lam coupling proceeds through a copper(II) to copper(0) catalytic cycle, or if it proceeds through a copper(II), copper(III), copper(I) process and then, in the presence of ambient air oxygen if this copper(I) species is then recycled to copper(0), restarting the cycle. Nevertheless, the catalytic cycle is characterized by de facto (I) ligand exchange, (II) transmetallation, (III) reductive elimination, and (IV) oxidation. A recent example of the Chan–Lam coupling to synthesize biologically active compounds is shown below: Compound 1, a pyrrolic amine, is coupled with aryl boronic ester, 2, to afford product 3, which is then carried forward to the biologically active target 4. The nitrile group of 2 does not poison the Cu(OAc)2 used, and pyridine is the ligand used for the reaction. Though the reaction is characterized by a lengthy duration (three days), it was carried out at room temperature in ambient air and resulted in a net 93% yield.".
- Chan-Lam_coupling wikiPageExternalLink JLA_CopperMechanisticStudies.pdf.
- Chan-Lam_coupling wikiPageID "44610362".
- Chan-Lam_coupling wikiPageLength "3938".
- Chan-Lam_coupling wikiPageOutDegree "16".
- Chan-Lam_coupling wikiPageRevisionID "683212219".
- Chan-Lam_coupling wikiPageWikiLink Alcohol.
- Chan-Lam_coupling wikiPageWikiLink Amine.
- Chan-Lam_coupling wikiPageWikiLink Boronic_acid.
- Chan-Lam_coupling wikiPageWikiLink Buchwald–Hartwig_amination.
- Chan-Lam_coupling wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Chan-Lam_coupling wikiPageWikiLink Category:Name_reactions.
- Chan-Lam_coupling wikiPageWikiLink Copper.
- Chan-Lam_coupling wikiPageWikiLink Copper(II)_acetate.
- Chan-Lam_coupling wikiPageWikiLink Ether.
- Chan-Lam_coupling wikiPageWikiLink Nitrile.
- Chan-Lam_coupling wikiPageWikiLink Palladium.
- Chan-Lam_coupling wikiPageWikiLink Pharmaceutical_drug.
- Chan-Lam_coupling wikiPageWikiLink Pyridine.
- Chan-Lam_coupling wikiPageWikiLink Tetrahedron_Letters.
- Chan-Lam_coupling wikiPageWikiLink File:ChanLamCouplingReaction1.pdf.
- Chan-Lam_coupling wikiPageWikiLink File:Chanlamreactionexamplebellstein.pdf.
- Chan-Lam_coupling wikiPageWikiLinkText "Chan-Lam coupling".
- Chan-Lam_coupling name "Chan-Lam coupling".
- Chan-Lam_coupling namedafter "Dominic Chan".
- Chan-Lam_coupling namedafter "Patrick Lam".
- Chan-Lam_coupling type "Coupling reaction".
- Chan-Lam_coupling wikiPageUsesTemplate Template:Nofootnotes.
- Chan-Lam_coupling wikiPageUsesTemplate Template:Reactionbox.
- Chan-Lam_coupling wikiPageUsesTemplate Template:Reactionbox_Identifiers.
- Chan-Lam_coupling wikiPageUsesTemplate Template:Reflist.
- Chan-Lam_coupling subject Category:Carbon-carbon_bond_forming_reactions.
- Chan-Lam_coupling subject Category:Name_reactions.
- Chan-Lam_coupling hypernym Reaction.
- Chan-Lam_coupling type Disease.
- Chan-Lam_coupling comment "The Chan–Lam coupling reaction – also known as the Chan–Evans–Lam coupling, as Chan, Evans, and Lam published their work back-to-back in Tetrahedron Letters – is a cross-coupling reaction between an aryl boronic acid and an alcohol or an amine to form the corresponding secondary aryl amines or aryl ethers, respectively. The Chan–Lam coupling is catalyzed in the presence of copper(II) species and may be conducted in air at room temperature.".
- Chan-Lam_coupling label "Chan-Lam coupling".
- Chan-Lam_coupling sameAs m.012fmnh9.
- Chan-Lam_coupling wasDerivedFrom Chan-Lam_coupling?oldid=683212219.
- Chan-Lam_coupling isPrimaryTopicOf Chan-Lam_coupling.