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Organic superbases are mostly charge-neutral, nitrogen containing species, where nitrogen act as a proton acceptor. These include the phosphazenes, phosphanes , amidines, and guanidines. Other organic compounds that meet the physicochemical or structural definitions of 'superbase' include proton chelators like the aromatic proton sponges and ...
The high reactivity of Schlosser's base is exploited in synthetic organic chemistry for the preparation of organometallic reagents. For example, potassium benzyl can be prepared from toluene using this reagent. Benzene and cis/trans-2-butene are also readily metalated by Schlosser's base. Toluene, benzene, and butenes react only slowly with ...
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