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Aryl reduction

Thieno[3,4-6]benzofuran, aryl-reduction, 4, 1074 Thieno[3,4-6]benzofurans synthesis, 4, 1074 Thienobenzo thiophenes synthesis, 4, 758... [Pg.879]

DeWeerd KA, JM Suflita (1990) Anaerobic aryl reductive dehalogenation of halobenzoates by cell extracts of Desulfomonile tiedjei. Appl Environ Microbiol 56 2999-3005. [Pg.504]

Kamikawa et al. chose the first option to generate the benthocyanin skeleton [91]. To begin with, 100 and aniline 126 are transformed into o-nitrodi-phenylamine 127 by intermolecular N-arylation. Reduction of the nitro group and selective bromination produces 128, and this time an intramolecular Buch-wald-Hartwig reaction is used to derive a mixture of the desired phenazine 129 and the elimination product 130. The fundamental problem with this approach relates to the selective introduction of the halogen substituent that is required for the intramolecular N-arylation. [Pg.108]

Reductive elimination of Caikyi-Caryi bonds can take place when /3-hydride elimination is blocked. As shown in Scheme 10, /3-aryl reductive elimination occurs in neophyl, -CH2CMe2Ph, complexes. This reaction is a rare example of unstrained C-C bond activation in organopalladium chemistry. [Pg.3555]

Ahring, B.K., N. Christiansen, I. Mathrani, H.V. Henriksen, A.J.L. Macario, and E.C. de Macario. 1992. Introduction of a de novo bioremediation ability, aryl reductive dechlorination, into anaerobic granular sludge by inoculation of sludge with Desulfomonile tiedjei. Appl. Environ. Microbiol. 58 3677-3682. [Pg.29]

Yahav-Levi A, Goldberg I, Vigalok A, Vedernikov AN (2008) Competitive aryl-iodide vs. aryl-aryl reductive elimination reactions in Pt(IV) Complexes experimental and theoretical studies. J Am Chem Soc 130 724—731... [Pg.120]


See other pages where Aryl reduction is mentioned: [Pg.732]    [Pg.395]    [Pg.732]    [Pg.732]    [Pg.732]    [Pg.277]    [Pg.71]    [Pg.215]   
See also in sourсe #XX -- [ Pg.136 ]

See also in sourсe #XX -- [ Pg.166 ]




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3.5.5- Tris-aryl-2 -furanones, reduction

Acrylic acids, 3-aryl, reduction

Alkene reductive arylations

Alkenes reductive coupling with aryl halides

Alkyl aryl ethers, reduction

Alkyl aryl sulfoxides reduction

Aryl aldehydes, reductive coupling

Aryl aldehydes, reductive coupling addition

Aryl aldehydes, reductive coupling bromides

Aryl aldehydes, reductive coupling reaction

Aryl aldimines, reduction

Aryl alkyl ketone, reduction

Aryl alkyl ketones reductive amination

Aryl alkylation, reductive

Aryl amines reductive elimination

Aryl azides, reduction

Aryl chlorides, reduction

Aryl complexes reduction

Aryl derivatives reductive elimination reactions

Aryl diethyl phosphates, reductive cleavage

Aryl ethers, reduction

Aryl ethers, reductive lithiation

Aryl fluorides reduction

Aryl hahdes, reductive coupling

Aryl halide reduction, single electron

Aryl halide, reduction

Aryl halides reductive

Aryl halides, reduction with organotin

Aryl halides, reduction with organotin hydride

Aryl ketimines, reductions

Aryl ketones, Meerwein-POnndorf-Verley reduction

Aryl ketones, reductive coupling

Aryl ketones, silane reduction

Aryl thiocyanates, reduction

Aryl triflates reduction

Aryl trifluoromethyl ketones reduction

Aryl-oxygen bonds, reductive cleavage

Biaryl synthesis aryl halide reductive coupling

Birch reduction aryl ethers

Diazonium salts aryl, reduction

Diazonium salts, aryl reduction, reagents

Ethanol reduction of aryl diazonium salts

Ethylenes, aryl-substituted, reduction

From Aryl Tellurium Trihalides by Reduction

Halides aryl, reductive coupling

Ketones, aryl reduction

Mizoroki reductive arylations

Palladium reductive arylations

Phosphate esters aryl, reduction

REDUCTION OF DIAZONIUM COMPOUNDS. ARYL HYDRAZINES

Radical reductive aryl

Reduction aryl alkyl

Reduction of Alkyl, Alkenyl, and Aryl Halides

Reduction of Aryl Ketones

Reduction of aryl diazonium ions

Reduction of aryl diazonium salts

Reduction of aryl nitro compound

Reduction prochiral aryl alkyl

Reductive Coupling Reactions of Aryl Aldehydes

Reductive Eliminations to Form -X Bonds from Aryl and Alkylplatinum(IV) Complexes

Reductive Mizoroki-Heck-Type Arylation in Action

Reductive Mizoroki-Heck-Type Arylations

Reductive dimerization of aryl halides

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