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Alkylative addition

G. Carbon on the Other Side 15-18 Addition of Alkanes Hydro-alkyl-addition... [Pg.1017]

O-Hydro, C-Alkyl Addition - Crignard Reaction (Mg Alkylation)... [Pg.517]

Despite considerable efforts, the formulation in equation (42) remains incomplete owing to the high reactivity of organocuprates as well as their oligomeric nature. Accordingly, we select organoborates as stable electron donors to study alkyl additions to various pyridinium acceptors (by thermal and photoinduced electron transfer) via charge-transfer salts as follows. [Pg.247]

The Addition of Boranes to Activated Double Bonds Hydro-alkyl-addition (overall transformation)... [Pg.803]

The Addition of Organometallic Compounds to Aldehydes and Ketones O-Hydro-C-alkyl-addition... [Pg.920]

The Formation of Metalated Aldimines 1 /1 /Lithio-alkyl-addition... [Pg.981]

Alkylation of allylic halides and alcohols (8, 334 335). Complete details of the reaction of RC.u BF3 with allylic halides and alcohols are now available. The reagent is probably an ate complex, RBF3 Cu 1, at least at low temperatures. In the case of allylic halides, THF is superior to ether for effecting /-substitution. However use of ether is essential for the direct alkylation. Addition of BF3 (even 2 equivalents) has no effect on reactions of C6II5Cu.5... [Pg.282]

ALKYLATION. Addition of an alkyl group. These reactions are important throughout synthetic organic chemistry for example, in the production of gasoline with high antiknock ratings for automobiles or for use in aircraft. [Pg.55]


See other pages where Alkylative addition is mentioned: [Pg.44]    [Pg.1024]    [Pg.1027]    [Pg.1031]    [Pg.1032]    [Pg.1182]    [Pg.1205]    [Pg.1209]    [Pg.1211]    [Pg.1216]    [Pg.1217]    [Pg.1239]    [Pg.1252]    [Pg.520]    [Pg.320]    [Pg.282]    [Pg.456]    [Pg.280]    [Pg.299]    [Pg.818]    [Pg.270]    [Pg.278]    [Pg.107]    [Pg.317]    [Pg.107]    [Pg.160]    [Pg.790]    [Pg.265]    [Pg.409]    [Pg.147]   


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1/1/Lithio-alkyl-addition

Acetylide Alkylation and Addition

Acid catalyzed, addition Friedel-Crafts alkylation

Addition alkylated pseudoephedrine amides

Addition alkylation

Addition alkylation

Addition of Alkyl Groups

Addition of alkyl halides

Addition of two alkyl groups

Addition reactions 3-hydroxy alkyl)mercury

Addition reactions, equilibria and alkyl radical heats of formation

Addition to perfluoroalkylalkynes alkylation at carbon

Addition with Tandem Alkylation

Addition, 1,3-dipolar, alkyl

Addition, 1,3-dipolar, alkyl azides

Addition-Alkylation Route to Prostaglandins

Additional Alkyl Groups

Aldehydes zinc alkyl addition

Alkanes, addition from alkyl halides

Alkanes, addition organometallics with alkyl

Alkyl addition reactions

Alkyl addition, aromatic ring, effect

Alkyl group oxidative addition

Alkyl groups addition reactions

Alkyl groups conjugate additions

Alkyl groups, nickel-catalyzed addition

Alkyl halides carbon monoxide addition

Alkyl halides from addition reactions

Alkyl halides oxidative addition

Alkyl halides, formation addition

Alkyl hydroperoxides alkene addition

Alkyl iodides, intermolecular radical addition

Alkyl lithium, asymmetric addition

Alkyl oxidative addition

Alkyl radical addition

Alkyl radical addition-cyclization

Alkyl radical additions to double and triple bonds

Alkyl radicals, conjugate addition

Alkyl zinc. enantioselective addition

Alkyl, Alkenyl, and Alkynyl Group Additions

Alkyl-Selective Addition to Ketones

Alkyl-halo-addition

Alkylating reagents, addition

Alkylation Friedel-Crafts addition

Alkylation Michael-type addition

Alkylation Reactions Electrophilic Addition

Alkylation and Addition Reactions

Alkylation by Conjugate Addition

Alkylation by conjugate addition reactions

Alkylation of Carbon Nucleophiles by Conjugate Addition

Alkylation of Carbon by Conjugate Addition

Alkylation, enolate ions electrophilic addition reactions

Alkylations and Additions of Other C-Nucleophiles to Imines

Aromatic compounds, addition alkyl substituents

Asymmetric Friedel-Crafts alkylation reactions Michael addition

Barbier additions alkyl halides

Basicity Addition of Alkyl or Acyl Ions

Benzene, alkyloxidative degradation via alkyl radical addition

Carbonyl addition/alkylation reaction

Conjugate Addition-Alkylation Route to Prostaglandins

Conjugate addition alkylation

Conjugate addition followed by alkylation

Conjugate addition with tandem alkylation

Cyclopentanone, 2,3-dialkylsynthesis conjugate addition-enolate alkylation

Cyclopropane, keto vinylfree radical 1,6-addition reactions alkyl boranes

Direct Oxidative Addition of Reactive Zinc to Functionalized Alkyl, Aryl, and Vinyl Halides

Electrophilic addition reactions Friedel-Crafts alkylation

Enamines, alkylation Michael additions

Enantioselective Alkylations and Additions of Other C -nucleophiles to Imines

Enantioselective allylic alkylations additions

Enones conjugate addition-enolate alkylation

Exchange Reactions of Group III Alkyl Addition Compounds

Food additives alkylating agents

Halides, alkyl, addition

Halides, alkyl, addition alkenes, Friedel-Crafts

Halides, alkyl, addition catalysts

Halogenated alkyl radical additions to double and triple bonds

Hydro-alkyl-addition

Imides, alkylation conjugate addition

Intramolecular, addition Friedel-Crafts alkylation

Isocyanates, addition from alkyl halides

Ketones alkyl group addition

Ketones axial selectivity of alkyl addition

Kinetic studies, alkyl electrophile oxidative addition

Lactams, alkylation conjugate addition

Leaded lead alkyl additive

Lithium alkyls, conjugate addition

Michael addition-allylic alkylation

Nitriles, acid catalyzed addition alkylation

O-hydro, C-alkyl addition

Organocuprates, addition with alkyl halides

Organolithium reagents, addition from alkyl halides

Organometallic compounds, 1,4-addition with alkyl-metal bonds

Organozinc compounds conjugate addition-alkylation

Oxidative Addition and Reductive Elimination of Alkyl Halides

Oxidative addition of alkyl halides

Oxidative addition, zinc metal alkyl bromides

Oxime ethers alkyl radical addition

Phenylsulfonyl oxime ethers, alkyl radical additions

Phosphines, alkylation metal catalyzed addition

Radical addition of alkyl radicals

Radical mechanism, addition with alkyl halides

Ruthenium addition-alkylation

Stereoselective alkyl addition

Tandem reactions addition-alkylation

Tandem reactions sulfone addition-alkylation

Zinc enolates conjugate addition-alkylation

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