Includes bibliographical references and index.
|Statement||edited by George A. Olah. Vol.4, Miscellaneous Reactions, Cumulative Indexes.|
|Contributions||Olah, George A. 1927-|
|The Physical Object|
|Number of Pages||1191|
Friedel–Crafts and related reactions The quinolizine derivative was obtained through a Friedel–Crafts acylation reaction onto the C-3 indole position of Friedel–Crafts and Related Reactions. The book covers the production and refining of Fischer-Tropsch syncrude to fuels and chemicals systematically and comprehensively, presenting a . Friedel-Crafts and Realted III. Part 2. Acylation and Related Reactions. Edition Hardcover – January 1, by George A. Olah (Author) See all formats and editions Hide other formats and editions. Price New from Used from Author: George A. Olah. Additional Physical Format: Online version: Olah, George A. (George Andrew), Friedel-Crafts and related reactions. New York, Interscience Publishers,
Friedel-Crafts and Related Reactions. vol. 2, parts 1 and 2, Alkylation and Related Reactions. George A. Olah, Ed. Interscience (Wiley), New York, Part 1, xxx Cited by: 2. The Friedel-Crafts acylation reaction is of interest to organic chemists in academia and industry. This work reviews the most important research on the Friedel-Crafts acylation reaction published during the past 30 years, and demonstrates how to make this reaction more economical and less damaging to the environment. ―Book News, June Cited by: Friedel–Crafts alkylation involves the alkylation of an aromatic ring with an alkyl halide using a strong Lewis acid, such as aluminium chloride, ferric chloride, or other MX n reagent, as catalyst. The general mechanism for tertiary alkyl halides is shown below.. For primary (and possibly secondary) alkyl halides, a carbocation-like complex with the Lewis acid, [R (+)(XMX n) RSC ontology ID: RXNO Friedel–Crafts dealkylation. Friedel–Crafts alkylation has been hypothesized to be a retro-Friedel–Crafts reaction or Friedel–Crafts dealkylation, alkyl groups are removed in the presence of protons or other Lewis acid.. For example, in a multiple addition of ethyl bromide to benzene, ortho and para substitution is expected after the first monosubstitution step because .
From inside the book. Friedel-Crafts and Related Reactions: Acylation and related reactions. 2 v compounds covalent Crafts crystalline dimer dissociation donor effect electron esters ether ethylene Friedel Friedel-Crafts catalysts Friedel-Crafts reactions Friedel-Crafts type gallium halogen heat hydrogen chloride hydrogen fluoride. Friedel-Crafts and related reactions / 1. General aspects.. Home. WorldCat Home About WorldCat Help. Search. Search for Library Items Search for Lists Search for Contacts Search for a Library. Create Book\/a>, schema:CreativeWork\/a> ; \u00A0\u00A0\u00A0 library. Heteropolyacids and large-pore zeolites as catalysts in acylation reactions using α,β-unsaturated organic acids as acylating agents C. De Castro, J. Primo and A. Corma 1 Sep | Journal of Molecular Catalysis A: Chemical, Vol. , No. A photochemical Alternative to the Friedel-Crafts Reaction. Abstract. The Friedel-Crafts reaction, a widely used reaction in both industrial and academic laboratories, produces several byproducts which must be handled as pollutants. An alternative which involves the photochemically-mediated reaction of an aldehyde with a quinone is described.