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Angewandte Chemie International Edition, ISSN 1433-7851, 02/2013, Volume 52, Issue 8, pp. 2217 - 2220
Inspiroation: A novel synthesis of spirocycles based on a palladium‐catalyzed intramolecular ipso‐Friedel–Crafts alkylation of phenols (see scheme;... 
oxidation | alkylation | palladium | spiro compounds | synthetic methods | Oxidation-Reduction | Phenols - chemistry | Molecular Structure | Catalysis | Indoles - chemistry | Palladium - chemistry | Alkylation | Palladium | Universities and colleges | Phenols | Synthesis | Indoles
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2019, Volume 58, Issue 23, pp. 7558 - 7598
Journal Article
Applied Catalysis A, General, ISSN 0926-860X, 2010, Volume 382, Issue 2, pp. 246 - 253
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2016, Volume 57, Issue 26, pp. 2868 - 2872
[Display omitted] •We develop firstly DBSA-catalyzed alkylation of olefins with alcohols in water.•DBSA-catalyzed alkylation of ketene dithioacetals and... 
Dodecylbenzenesulfonic acid | Ketene dithioacetals | Friedel–Crafts alkylation | Olefins | Alcohols | Friedel-Crafts alkylation | ROUTE | ACID CATALYSTS | BENZYLIC ALCOHOLS | ANNULATION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | ODORLESS | INDOLES | CARBON BOND FORMATION | THIOACETALIZATION | Water
Journal Article
Catalysis Communications, ISSN 1566-7367, 09/2017, Volume 100, pp. 38 - 42
In this paper, a simple and highly efficient Friedel–Crafts Michael–type addition of indoles to electron-deficient olefins was achieved by a new magnetic ionic... 
C[sbnd]C bond formation | Indoles | Friedel–crafts reaction | α,β-unsaturated ketones | Ionic liquid | C–C bond formation | ACID | ONE-POT SYNTHESIS | CHEMISTRY, PHYSICAL | ALPHA | GREEN | Friedel crafts reaction | HIGHLY EFFICIENT | MICHAEL ADDITION | C-C bond formation | alpha,beta-unsaturated ketones | FRIEDEL-CRAFTS ALKYLATION | DERIVATIVES | NITROALKENES | CONJUGATE ADDITION | Ketones | Olefins
Journal Article
Topics in Catalysis, ISSN 1022-5528, 06/2018, Volume 61, Issue 7-8, pp. 610 - 615
Crystalline syndiotactic polystyrene (sPS) was functionalized by superacid-catalyzed Friedel-Crafts alkylation. Once a tertiary carbocation is generated by the... 
Superacid | Friedel–Crafts alkylation | Crystalline polymer | Post-functionalization | Syndiotactic polystyrene | SULFONATED POLYSTYRENE | CRYSTALLIZATION | MELT | CHEMISTRY, PHYSICAL | POLYMERIZATION | STYRENE | Friedel-Crafts alkylation | COMBINATION | GLASS-TRANSITION | IONOMERS | CHEMISTRY, APPLIED | IONIC INTERACTIONS | Thermal properties | Crystalline polymers | Polystyrene | Alcohols
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 05/2019, Volume 60, Issue 19, pp. 1325 - 1329
[Display omitted] •Indoles may be alkylated by trichloroacetimidates with Lewis acids.•Benzylic and allylic imidates are most effective.•Electron poor imidates... 
Lewis acid | Friedel-Crafts | Indole | Alkylation | SUBSTITUTION | CATALYZED PROPARGYLATION | ALLYLATION | CHEMISTRY, ORGANIC | C-GLYCOSIDES | ALCOHOLS | MILD | FUNCTIONALIZATION | HETEROCYCLES | O-GLYCOSYL | DERIVATIVES
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 06/2017, Volume 55, Issue 12, pp. 1991 - 1997
Journal Article