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John E. McMurry (born July 27, 1942, in New York City) is Professor Emeritus in the Department of Chemistry and Chemical Biology at Cornell University. He received an A.B. from Harvard University in 1964 and his Ph.D. from Columbia University in 1967 working with Gilbert Stork .
The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent. The reaction is named after its co-discoverer, John E. McMurry.
McMurry3rd is for referencing the 3rd edition (1992) of Organic Chemistry by John E. McMurry. It is based on the template {}. Parameters are: page (optional): to reference a single page; pages (optional): to reference multiple pages
In organic chemistry, cheletropic reactions, also known as chelotropic reactions, [2] are a type of pericyclic reaction (a chemical reaction that involves a transition state with a cyclic array of atoms and an associated cyclic array of interacting orbitals). [1] Specifically, cheletropic reactions are a subclass of cycloadditions.
McMurry reaction; Meerwein arylation; Meerwein–Ponndorf–Verley reduction; Meisenheimer rearrangement; Meissenheimer complex; Menshutkin reaction; Metal-ion-catalyzed σ-bond rearrangement; Mesylation; Merckwald asymmetric synthesis; Metallo-ene reaction; Methylation; Meyer and Hartmann reaction; Meyer reaction; Meyer synthesis; Meyer ...
The Robinson annulation is a chemical reaction used in organic chemistry for ring formation. It was discovered by Robert Robinson in 1935 as a method to create a six membered ring by forming three new carbon–carbon bonds. [1]