Silyl enol ether — Silyl enol ethers in organic chemistry are a class of organic compounds sharing a common functional group composed of an enolate bonded through its oxygen terminus to an organosilicon group.Silyl enol ethers are important intermediates in organic … Wikipedia
Ether lipid — Ether lipids are lipids in which one or more of the carbon atoms on glycerol is bonded to an alkyl chain via an ether linkage, as opposed to the usual ester linkage. TypesEther lipids are called plasmalogens (1 O 1 alkenyl 2… … Wikipedia
Éther d'énol — La structure du groupe éther d énol. Un éther d’énol est un alcène avec un substituant alkoxy donc de structure générale R1R2C=CR3–O–R4 avec R un groupe alkyle ou aryle. Les éthers d énol comme les énamines sont des alcènes activés ou alcènes… … Wikipédia en Français
Keto-Enol-Tautomerie — Die Tautomerie (von gr. tautó = das Gleiche; gr. meros = der Anteil) bezeichnet in der Chemie eine besondere Form der Isomerie. Sie wurde 1876 von Alexander Michailowitsch Butlerow (1828–1886) entdeckt und 1885 von Conrad Peter Laar als Begriff… … Deutsch Wikipedia
Keto-enol tautomerism — In organic chemistry, keto enol tautomerism refers to a chemical equilibrium between a keto form (a ketone or an aldehyde) and an enol. The enol and keto forms are said to be tautomers of each other. The interconversion of the two forms involves… … Wikipedia
Methyl vinyl ether — Other names Methoxyethene, ethenyl methyl ether, vinyl methyl ether … Wikipedia
Silyl ether — General structure of a silyl ether Silyl ethers are a group of chemical compounds which contain a silicon atom covalently bonded to an alkoxy group. The general structure is R1R2R3Si−O−R4 where R4 is an alkyl group or an aryl group. Silyl ethers… … 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
Mukaiyama aldol addition — The Mukaiyama aldol addition is an organic reaction and a type of aldol reaction between a silyl enol ether and an aldehyde catalyzed by a Lewis acid.[1] This choice of reactants allows for a crossed aldol reaction between an aldehyde and a… … Wikipedia
Kuwajima Taxol total synthesis — This synthesis is truly synthetic without any help from small biomolecule precursors and also a linear synthesis with molecule ring construction in the order of A, B, C, D. At some point chirality is locked into the molecule via an asymmetric… … Wikipedia
