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Stannanes aryl, electrophilic substitution reactions

The P-effect similarly enhances the reactivity of alkynyl- (Section 8.2.2), alkenyl-(Section 8.1.2), allyl- (Section 9.1.3.2), and aryl- (Section 7.1) stannanes in their reactions with electrophiles (equations 3-33-3-36), and its effect can be recognised in other contexts such as the ene reactions of allylstannanes (Section 9.1.3.4), and the charge-transfer reactions and ring-substitution reactions of benzylstannanes.22... [Pg.37]

Tin, zinc, boron, and mercury metallopyrimidines in alkylation and arylation reactions Acylation by electrophilic substitution Acylation by palladium-catalyzed reactions with stannanes Tin metallopyrimidines in acylation reactions Coupling reactions in quinazolines and perimidines Alkylation and arylation by organometallic adduct formation... [Pg.94]

See other pages where Stannanes aryl, electrophilic substitution reactions is mentioned: [Pg.564]    [Pg.9]    [Pg.445]    [Pg.445]    [Pg.361]    [Pg.4879]    [Pg.445]    [Pg.445]    [Pg.445]    [Pg.341]   
See also in sourсe #XX -- [ Pg.589 ]

See also in sourсe #XX -- [ Pg.579 ]

See also in sourсe #XX -- [ Pg.589 ]



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Aryl electrophiles

Aryl substituted

Aryl-substitution

Electrophilic substitution arylation

Electrophilic substitution reaction

Stannane reactions

Stannanes reactions

Stannanes, aryl

Substitution reactions electrophile

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