Alkylation of aromatic compounds with pummerer rearrangement intermediates. Application to the preparation of methyl-aryl compounds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles.
2. Carbocationic and related processes in reactions of .alpha.-keto mesylates and triflates
3. The indole 2-3-quinodimethane strategy for the synthesis of indole alkaloids
4. Electrophilic methylthiomethylation of enol ethers and activated aromatic compounds. Application of the former reaction to the synthesis of the macrocycle, 3,3,7,7,11,11,15,15-octamethyl-1,9-dithia-5,13-diaza-cyclohexadecane
5. Aromatic electrophilic substitution by Pummerer rearrangement intermediates
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1. On Aromatic Electrophilic Substitution Promoted by In Situ Generated Thionium Ions;Synthesis;2013-02-27
2. A novel NH4OAc and CuBr(PPh3)3-induced intermolecular Pummerer-type reaction between free (NH)-indoles and dimethylsulfoxide: facile synthesis of 3-methylthiomethyl substituted indoles;Tetrahedron;2012-02
3. Active thionium species mediated functionalization at the 2α-position of indole derivatives;Chemical Communications;2011
4. Sulfones and Sulfoxides;Ullmann's Encyclopedia of Industrial Chemistry;2000-06-15
5. New Application of the Pummerer Reaction of Imidosulfoxides for the Generation of Mesoionic Dipoles;The Journal of Organic Chemistry;1997-02-01
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