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Amide Bond Activation

dc.contributor.authorSzostak, Michal*
dc.date.accessioned2021-02-11T08:07:44Z
dc.date.available2021-02-11T08:07:44Z
dc.date.issued2019*
dc.date.submitted2019-08-28 11:21:27*
dc.identifier35900*
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/40763
dc.description.abstractThe amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical transformations of amides. These developments cover an impressive range of catalytic N–C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations. Equally relevant are structural and theoretical studies that provide the basis for chemoselective manipulation of amidic resonance. This monograph on amide bonds offers a broad survey of recent advances in activation of amides and addresses various approaches in the field.*
dc.languageEnglish*
dc.subjectQD1-999*
dc.subjectQ1-390*
dc.subjectQD450-801*
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PN Chemistryen_US
dc.subject.otherN-heterocyclic carbene*
dc.subject.othernon planar amide*
dc.subject.otherruthenium (Ru)*
dc.subject.otherphysical organic chemistry*
dc.subject.othergemcitabine prodrug*
dc.subject.otherpyramidal amides*
dc.subject.otherbridged sultams*
dc.subject.othercatalysis*
dc.subject.otherdipeptides*
dc.subject.otherN-(1-naphthyl)acetamide*
dc.subject.otherC-N ? bond cleavage*
dc.subject.othersteric effects*
dc.subject.otherpeptide bond cleavage*
dc.subject.othertransition-metal-free*
dc.subject.otherpalladium*
dc.subject.otherN-heterocyclic carbenes (NHCs)*
dc.subject.otheraddition reaction*
dc.subject.otherC–O activation*
dc.subject.otherrhodium*
dc.subject.othermetal complexes*
dc.subject.othercarbanions*
dc.subject.otherthioamidation*
dc.subject.otheramide bond*
dc.subject.otherintramolecular catalysis*
dc.subject.otherantiviral activity*
dc.subject.otheradditivity principle*
dc.subject.otherpre-catalysts*
dc.subject.otherC–N bond cleavage*
dc.subject.otherbridged lactams*
dc.subject.otherC–H acidity*
dc.subject.otherarynes*
dc.subject.othertwisted amides*
dc.subject.otherorganic synthesis*
dc.subject.otheramination*
dc.subject.otherSuzuki-Miyaura*
dc.subject.othertert-butyl*
dc.subject.othercyclopentadienyl complexes*
dc.subject.otherC-S formation*
dc.subject.otherenzymes*
dc.subject.otherDFT study*
dc.subject.othersulfonamide bond*
dc.subject.otherN*
dc.subject.otherHERON reaction*
dc.subject.otherprimaquine*
dc.subject.otherentropy*
dc.subject.otheramide activation*
dc.subject.otheramidation*
dc.subject.othersynthesis*
dc.subject.otheramide hydrolysis*
dc.subject.othercarbonylicity*
dc.subject.otheramide bond activation*
dc.subject.otheramide bond resonance*
dc.subject.otheraminosulfonylation*
dc.subject.othermolecular dynamics*
dc.subject.othermodel compound*
dc.subject.otherin situ*
dc.subject.otheramide*
dc.subject.otherhomogeneous catalysis*
dc.subject.otherheterocycles*
dc.subject.otheranomeric effect*
dc.subject.othermulti-component coupling reaction*
dc.subject.otherkinetic*
dc.subject.otherexcited state*
dc.subject.otherC–H bond cleavage*
dc.subject.otherpalladium catalysis*
dc.subject.otheramides*
dc.subject.otherthiourea*
dc.subject.otherformylation*
dc.subject.otheralkynes*
dc.subject.othercis/trans isomerization*
dc.subject.otheramide C–N bond activation*
dc.subject.otherintein*
dc.subject.otherC-H functionalization*
dc.subject.othersuccindiamide*
dc.subject.otheramide bonds*
dc.subject.othercrown ether*
dc.subject.otheraminoacylation*
dc.subject.otherdirecting groups*
dc.subject.othercytostatic activity*
dc.subject.otherreaction thermodynamics*
dc.subject.otheracyl transfer*
dc.subject.othertransition metals*
dc.subject.otherN-dimethylformamide*
dc.subject.otherDMAc*
dc.subject.otheracylative cross-coupling*
dc.subject.otherC-H/C-N activation*
dc.subject.othernickel catalysis*
dc.subject.otherantibacterial screening*
dc.subject.othersodium*
dc.subject.otheraryl thioamides*
dc.subject.otherWinkler-Dunitz parameters*
dc.subject.othercatalyst*
dc.subject.otherN-dimethylacetamide*
dc.subject.otherbase-catalyed hydrolysis*
dc.subject.othernitrogen heterocycles*
dc.subject.othercross-coupling*
dc.subject.otherinsertion*
dc.subject.otheramidicity*
dc.subject.othernitro-aci tautomerism*
dc.subject.otheractivation*
dc.subject.othercarbonylation*
dc.subject.othertransamidation*
dc.subject.otheramine*
dc.subject.otherdistortion*
dc.subject.otherPd-catalysis*
dc.subject.otherrotational barrier energy*
dc.subject.otherhypersensitivity*
dc.subject.otherN–C activation*
dc.subject.othermetabolic stability*
dc.subject.other[2+2+2] annulation*
dc.subject.othertwisted amide*
dc.subject.otherprotease*
dc.subject.othercyanation*
dc.subject.otheramide resonance*
dc.subject.othertrialkylborane*
dc.subject.othercatalysts*
dc.subject.otherbiofilm eradication*
dc.subject.otherpharmacokinetics*
dc.subject.otherpancreatic cancer cells*
dc.subject.otherDMF*
dc.subject.otheraryl esters*
dc.subject.otherMichael acceptor*
dc.subject.otherfumardiamide*
dc.subject.otherwater solvation*
dc.subject.otherester bond activation*
dc.subject.othercyclization*
dc.subject.othernuclear magnetic resonance*
dc.subject.othersecondary amides*
dc.subject.otherreaction mechanism*
dc.subject.otherdensity functional theory*
dc.subject.otherdensity-functional theory*
dc.subject.otheramino acid transporters*
dc.titleAmide Bond Activation*
dc.typebook
oapen.identifier.doi10.3390/books978-3-03921-204-0*
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0*
oapen.relation.isbn9783039212033*
oapen.relation.isbn9783039212040*
oapen.pages466*
oapen.edition1st*


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