Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitro groups, conjugating effects carbanions

Many carbanionic nucleophiles that would be considered too hard to react as Michael donors can be made into effective reagents for conjugate addition reactions by appending resonance or inductively stabilizing groups to soften their intrinsic Lewis basicity. Such stabilized anionic Michael donors include enolates, alkylthio-substituted carbanions, ylides and nitro-substituted carbanions. [Pg.258]


See other pages where Nitro groups, conjugating effects carbanions is mentioned: [Pg.236]    [Pg.177]    [Pg.432]    [Pg.303]    [Pg.133]    [Pg.407]    [Pg.225]    [Pg.1228]    [Pg.284]    [Pg.133]    [Pg.625]    [Pg.310]    [Pg.203]   
See also in sourсe #XX -- [ Pg.625 ]




SEARCH



Carbanions nitro

Conjugative effects

Effects conjugation

Nitro group

Nitro groups, conjugating effects

© 2024 chempedia.info