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Alkynyl alkylation

In summary, the Pd-catalyzed alkynylation with alkynylzincs has finally become generally applicable with the exception of the alkynyl-alkyl coupling and often capricious... [Pg.505]

R = alkenyl, aryl, allyl, benzyl, propargyl R = alkenyl, aryl, alkynyl, alkyl, benzyl, allyl The Negishi Coupling was the first reaction that allowed the preparation of unsymmetrical biaryls in good yields. The versatile nickel- or palladium-catalyzed coupling of organozinc compounds... [Pg.165]

With regard to diorganozincs other than primary dialkylzincs, various diorganozincs such as divinylzinc (> 96% ee, addition to benzaldehyde),4 difurylzinc (72% ee, addition to benzaldehyde),5 diphenylzinc (78-82% ee, addition to various aldehydes),6 and diisopropylzinc (93% ee, addition to benzaldehyde)7 have been utilized in the chiral (3-aminoalcohol catalysed reactions. Alkenyl(alkyl)zincs4b,c and alkynyl(alkyl)zincs8 afford the corresponding chiral allylic and propargyl alcohols. [Pg.246]

Alkynyliodonium ions, 1 and 2, are hypervalent iodine species in which one or two alkynyl ligands are bound to a positively charged iodine(III) atom. They are sensitive to nucleophiles, especially at the /1-carbon atom(s) of the alkynyl ligand(s), and for that reason, the isolation of stable alkynyliodonium salts generally requires the incorporation of nucleofugic anions. A list of known alkynyliodonium compounds (i.e. as of 4/1/94), containing 134 iodonium salts derived from 103 iodonium ions, and references (5-45) to their preparation and characterization are presented in Table 1. Among these compounds, alkynyl(phenyl)iodonium sulfonates and tetrafluoroborates are the most common, while alkynyl(alkyl)iodonium salts of any kind are unknown. [Pg.1175]

Allyl > Benzyl, Acyl > Akenyl > Aryl simple Propargyl Alkynyl Alkyl... [Pg.132]

Alkynyl C—H Alkylations, C(sp)—Alkynyl-Alkyl Bond Formations. .. 192... [Pg.175]

ALKYNYL C—H ALKYLATIONS, C(sp)—H ALKYNYL-ALKYL BOND FORMATIONS... [Pg.192]

SYNTHESIS OF THIOETHERS, SULFONES, AND RELATED COMPOUNDS Example 5.5 Preparation of an Alkynyl Alkyl Sulfide [103],... [Pg.508]


See other pages where Alkynyl alkylation is mentioned: [Pg.392]    [Pg.146]    [Pg.289]    [Pg.131]    [Pg.134]    [Pg.178]    [Pg.326]    [Pg.302]    [Pg.260]    [Pg.288]    [Pg.316]    [Pg.19]    [Pg.392]    [Pg.27]    [Pg.26]    [Pg.192]    [Pg.33]    [Pg.92]    [Pg.60]    [Pg.288]    [Pg.33]    [Pg.284]    [Pg.252]   
See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.3 ]




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Alkyl, Alkenyl, and Alkynyl Group Additions

Alkyl-alkynyl coupling

Alkyl-substituted alkynyl

Alkyl-substituted alkynyl substrates

Alkylation alkynyl carbanions

Alkylation of alkynyl anions

Alkynyl group, alkyl stabilization

Cyanide, alkynyl and alkyl anions

Reaction of alkyl, alkenyl alkynyl and carbene ligands

Sulfides alkynyl alkyl

Tert-alkyl-alkynyl coupling

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