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Category

Superbases

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lithium hydride
chemical compound
sodium hydride
chemical compound
n-butyllithium
thumb|Glass bottles containing butyllithium '''n-Butyllithium C4H9Li (abbreviated n-BuLi''') is an organolithium reagent. It is widely used as a polymerization initiator in the production of elastomers such as polybutadiene or styrene-butadiene-styrene (SBS). Also, it is broadly employed as a strong base (superbase) in the synthesis of organic compounds, such as in the pharmaceutical industry.
potassium hydride
inorganic compound of potassium and hydride
tert-butyllithium
'''tert-Butyllithium' is a chemical compound with the formula (CH3)3CLi. As an organolithium compound, it has applications in organic synthesis since it is a strong base, capable of deprotonating many carbon molecules, including benzene. tert''-Butyllithium is available commercially as solutions in hydrocarbons (such as pentane); it is not usually prepared in the laboratory.
lithium diisopropylamide
chemical compound
superbase
A superbase is a compound that has a particularly high affinity for protons. Superbases are of theoretical interest and potentially valuable in organic synthesis. Superbases have been described and used since the 1850s.
amidines
thumb|right|150px|The structural formula of acetamidine (acetimidamide). Amidines are organic compounds with the functional group RC(NR)NR2, where the R groups can be the same or different. They are the imine derivatives of amides (RC(O)NR2). The simplest amidine is formamidine, HC(=NH)NH2.
rubidium hydride
chemical compound
caesium hydride
chemical compound
phosphazene
Phosphazenes refer to various classes of organophosphorus compounds featuring phosphorus(V) with a double bond between P and N. One class of phosphazenes have the formula . These phosphazenes are also known as iminophosphoranes and phosphine imides. They are superbases.
diethynylbenzene dianion
group of isomeric chemical compounds
Schlosser's base