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In addition to his scientific work, McMurry is the author of 45 undergraduate chemistry textbooks that have been translated into 12 languages and used throughout the world. McMurry's most popular textbook Organic Chemistry was first printed in 1984. In 2022, he sold the rights for the book to OpenStax making it free for the user.
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
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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.
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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]
The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted amides. [1] [2] The rearrangement has also been successfully performed on haloimines and nitrones.