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Angewandte Chemie International Edition, ISSN 1433-7851, 02/2020, Volume 59, Issue 9, pp. 3568 - 3572
A simple and ubiquitously present group, free amine, is used as a directing group to synthesize axially chiral biaryl compounds by PdII‐catalyzed... 
chiral spiro phosphoric acids | biaryl-2-amines | palladium | atroposelectivity | C−H olefination | Phosphates | Phosphoric acid | Amines | Chemical industry | Ligands
Journal Article
Angewandte Chemie (International ed. in English), ISSN 1433-7851, 02/2020, Volume 59, Issue 9, pp. 3568 - 3572
A simple and ubiquitously present group, free amine, is used as a directing group to synthesize axially chiral biaryl compounds by Pd -catalyzed... 
biaryl-2-amines | C(SP)-H BONDS | atroposelectivity | ACTIVATION | ENANTIOSELECTIVE SYNTHESIS | BIARYL COMPOUNDS | ARYLATION | chiral spiro phosphoric acids | CHEMISTRY, MULTIDISCIPLINARY | ATROPISOMERS | LIGANDS | C-H olefination | palladium | STEREOSELECTIVE-SYNTHESIS | C(SP)-H | ALKENYLATION
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2012, Volume 354, Issue 2‐3, pp. 347 - 353
A new, general method for the synthesis of phenanthridines has been developed by palladium‐catalyzed oxidative remote CH olefination–carboamination–CC bond... 
palladium | phenanthridines | biaryl‐2‐amines | alkenes | oxidative CC bond cleavage | biaryl-2-amines | oxidative C-C bond cleavage | SUBSTITUTION | DIRECT ARYLATION | COMPLEXES | CHEMISTRY, ORGANIC | H ACTIVATION | BENZYL | COUPLING REACTIONS | ARYL | CHEMISTRY, APPLIED | HECK REACTION | oxidative C?C bond cleavage | DERIVATIVES | ALKALOIDS
Journal Article
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