- organocopper
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organocopper
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Organocopper compound — Lithium diphenylcuprate etherate dimer from crystal structure … Wikipedia
Copper — For other uses, see Copper (disambiguation) … Wikipedia
Gilman reagent — General structure of a Gilman reagent A Gilman reagent is a lithium and copper (diorganocopper) reagent compound, R2CuLi, where R is an organic radical. These are useful because they react with organic chlorides, bromides, and iodides to replace… … Wikipedia
Cuprate — For cuprate superconductors, see High temperature superconductivity#Cuprates. The unit cell of high temperature cuprate superconductor BSCCO 2212 Cuprates (from Latin cuprum meaning copper) are chemical compounds containing copper anion. Cuprates … Wikipedia
Copper(I) chloride — IUPAC name Copper(I) chloride … Wikipedia
Organometallic chemistry — n Butyllithium, an organometallic compound. Four lithium atoms are shown in purple in a tetrahedron, and each lithium atom is bound to a butyl group (carbon is black, hydrogen is white). Organometallic chemistry is the study of chemical compounds … Wikipedia
Methyllithium — IUPAC name Methyllithium … Wikipedia
Gilman reagent — ▪ chemistry another name for organocopper compounds used for carbon carbon bond formation in organic synthesis. Compounds of this type were first described in the 1930s by the American chemist Henry Gilman, for whom they are named. The most … Universalium
Ketone — group … Wikipedia
Alkylation — Alkylating agent redirects here. For the class of drugs, see alkylating antineoplastic agent. Alkylation is the transfer of an alkyl group from one molecule to another. The alkyl group may be transferred as an alkyl carbocation, a free radical, a … Wikipedia
