Big Chemical Encyclopedia

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

Articles Figures Tables About

Monometallic organolithium reagents

As outlined in the following text, the halogen/metal exchange is an equilibrium, and thus the position of the equilibrium depends on the basicity of the exchange reagent, fert-butyllithium outperforms 5ec-butylhthium, which is superior to butyUithium. Methylhthium is the least reactive alkyhithium reagent but can stiU be more effective than phenylhthium in some cases  [Pg.814]

Hetero-substituents such as dialkylamino or bis(trialkylsilyl)amino, alkoxy and 2-tetrahydro-pyranyloxy, lithiooxy or lithiooxycarbonyl, fluoro or trifluoromethyl, and chloro are well tolerated. Cyano or nitro and bromo or iodo substituents are tolerated when the solvent and temperature are carefully chosen [3]. [Pg.814]


See other pages where Monometallic organolithium reagents is mentioned: [Pg.814]    [Pg.814]    [Pg.208]    [Pg.169]   
See also in sourсe #XX -- [ Pg.814 ]




SEARCH



Monometallic

Organolithium reagents

Organolithiums reagents

© 2024 chempedia.info