lithium alkoxide

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• Alkoxide — The structure of a typical alkoxide group. An alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. They can be written as RO−, where R is the organic substituent.… …   Wikipedia

• Lithium amide — Chembox new ImageFile = ImageSize = IUPACName = Lithium amide OtherNames = Lithamide Section1 = Chembox Identifiers CASNo = 7782 89 0 PubChem = SMILES = Section2 = Chembox Properties Formula = LiNH2 MolarMass = 22.96 g/mol Appearance = white… …   Wikipedia

• Lithium diisopropylamide — Chembox new Name = Lithium diisopropylamide ImageFile = lithium diisopropylamide.png ImageSize = 150px ImageName = Lithium diisopropylamide IUPACName = Lithium diisopropylamide OtherNames = LDA Section1 = Chembox Identifiers SMILES = CC(C) [N ]… …   Wikipedia

• Acetylide — Identifiers ChemSpider 6113  Y Jmol 3D images …   Wikipedia

• Methylation — In the chemical sciences, methylation denotes the addition of a methyl group to a substrate or the substitution of an atom or group by a methyl group. Methylation is a form of alkylation with, to be specific, a methyl group, rather than a larger… …   Wikipedia

• Metal acetylide — A metal acetylide is an alkyne for which the terminal proton (hydrogen) has been replaced by a metal such as sodium or an organolithium. So, for example, the alkyne CH3C≡CH could be deprotonated to form the acetylide ion CH3C≡C−. Once it has been …   Wikipedia

• 1,2-Wittig rearrangement — A 1,2 Wittig rearrangement is a categorization of chemical reactions in Organic chemistry, and consists of a 1,2 rearrangement of an ether with an alkyllithium compound [Georg Wittig, L. Löhmann, Ann. 550, 260 (1942)] [G. Wittig, Experientia 14,… …   Wikipedia

• Holton Taxol total synthesis — The Holton Taxol total synthesis, published by Robert A. Holton and his group at Florida State University in 1994 was the first total synthesis of Taxol (generic name: paclitaxel) [ First total synthesis of taxol 1. Functionalization of the B… …   Wikipedia

• Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

• carboxylic acid — Chem. any organic acid containing one or more carboxyl groups. [1900 05; CARBOXYL + IC] * * * Any organic compound with the general chemical formula ―COOH in which a carbon (C) atom is bonded to an oxygen (O) atom by a double bond to make a… …   Universalium

• Saponification — of a triglyceride with sodium hydroxide. Saponification is a process that produces soap, usually from fats and lye. In technical terms, saponification involves base (usually caustic soda NaOH) hydrolysis of triglycerides, which are esters of… …   Wikipedia