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Journal of heterocyclic chemistry, ISSN 0022-152X
Journal
Tetrahedron, ISSN 0040-4020, 06/2018, Volume 74, Issue 26, pp. 3318 - 3324
The synthesis of bridgehead fused [5,6]-bicyclic heterocycles via rhodium(III)-catalyzed C–H functionalization of C-alkenyl azoles with sulfoxonium ylides is... 
Catalysis | Rhodium | Nitrogen heterocycle | C–H functionalization | Sulfoxonium ylide | ANNULATIONS | ACTIVATION | INSERTION | PHARMACEUTICALS | BOND FUNCTIONALIZATIONS | CHEMISTRY, ORGANIC | DIAZO-COMPOUNDS | C-H functionalization | ALKYNES | CLEAVAGE | Chemical synthesis
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2015, Volume 21, Issue 49, pp. 17860 - 17869
An unusual, highly‐strained annulated 2,2′‐biimdazole was isolated as decomposition product of the outer‐sphere one‐electron oxidation of an iron(II)... 
oxidation | iron | reductive elimination | biimidazolium | nitrogen heterocycles | NONHEME IRON | ORGANIC-SYNTHESIS | ACTIVATION | ELECTRON-DONOR | CHEMISTRY, MULTIDISCIPLINARY | EPOXIDATION | CROSS-COUPLING REACTIONS | CHEMISTRY | H BONDS | CATALYTIC-ACTIVITY | Pyridines | Ligands | Activation | Formations | Oxidation | Decomposition | Coordination compounds | Carbenes
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2019, Volume 58, Issue 5, pp. 1458 - 1462
Methods that provide rapid access to new heterocyclic structures in biologically relevant chemical space provide important opportunities in drug discovery.... 
cyclization | rhodium catalysis | amino acids | nitrogen heterocycles | fragment synthesis | Organic chemistry | Rhodium | Bioactive compounds | Aromatic compounds | Insertion | Amino acids | Nitrogen | Stitching | Biological activity
Journal Article
Catalysis Reviews, ISSN 0161-4940, 01/2015, Volume 57, Issue 1, pp. 1 - 78
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2017, Volume 359, Issue 10, pp. 1631 - 1636
An easily prepared oxalic diamide is a powerful ligand for the copper‐catalyzed coupling of aryl halides with nitrogen heterocycles. Only 1–2 mol% each of... 
coupling | aryl halides | low catalytic loading | copper salts | nitrogen heterocycles | EFFICIENT LIGAND | C-N | BOND-FORMING REACTIONS | CHEMISTRY, ORGANIC | HETEROARYL HALIDES | HIGHLY EFFICIENT | MILD CONDITIONS | CROSS-COUPLINGS | EXCELLENT LIGAND | CHEMISTRY, APPLIED | N-ARYLATION | Cytokinins | Copper oxide | Copper | Halides | Cuprite | Catalysis | Coupling | Nitrogen | Aromatic compounds
Journal Article