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Chemical Society Reviews, ISSN 0306-0012, 6/2011, Volume 4, Issue 7, pp. 343 - 3444
The [2+2+2] cycloaddition is an elegant, atom-efficient and group tolerant process for the synthesis of carbo- and heterocycles, mostly aromatic, involving the... 
N-H ACTIVATION | ALKENES | REGIOSELECTIVE CYCLOTRIMERIZATION | ENANTIOSELECTIVE SYNTHESIS | AXIAL CHIRALITY | CONSTRUCTION | COBALT-CATALYZED CYCLOTRIMERIZATION | ALKYNE CYCLOTRIMERIZATION | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | C-H
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2011, Volume 50, Issue 46, pp. 10917 - 10921
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 2019, Volume 58, Issue 11, p. 3466
While the coordination chemistry of monometallic complexes and the surface properties of extended metal particles are well understood, the control of metal... 
cubanes | cyclotrimerization | hydrogenation | manganese | alkynes
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2015, Volume 2015, Issue 2, pp. 265 - 286
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 12/2018, Volume 59, Issue 49, pp. 4311 - 4314
Two different pathways for the synthesis of annulated pyrido[3,4- ]indoles are reported using metal-catalyzed cyclotrimerization reactions. A stepwise process... 
Pyridoindole | Cyclotrimerization | Tandem catalysis | Multicomponent
Journal Article
Tetrahedron, ISSN 0040-4020, 2011, Volume 67, Issue 34, pp. 6095 - 6130
The main strategies for the synthesis of fused heterocycles by metal-mediated [2+2+2] cyclotrimerization of alkynes and/or nitriles as well as their specific... 
REGIOSELECTIVE CYCLOTRIMERIZATION | ONE-STEP SYNTHESIS | CATALYZED CYCLOADDITION | INTRAMOLECULAR CYCLOTRIMERIZATION | AQUEOUS-MEDIUM | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | 1,6-DIYNES | DERIVATIVES | 2,2'-BIPYRIDINE LIGANDS | COBALT | Nitriles | Universities and colleges
Journal Article
Tetrahedron, ISSN 0040-4020, 03/2019, Volume 75, Issue 10, pp. 1359 - 1363
We have demonstrated a useful synthetic strategy to assemble star-shaped -symmetric molecules containing 1,3-azole moieties at the periphery. To generate these... 
C3-symmetric | Cyclotrimerization | 1,3-Azoles | Heteroaryl Heck coupling
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2006, Volume 348, Issue 16‐17, pp. 2307 - 2327
Journal Article
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, ISSN 0002-7863, 06/2012, Volume 134, Issue 25, pp. 10515 - 10531
[Ir(cod)Cl](2)/DPPF or BINAP efficiently catalyzed the cycloaddition of alpha,omega-diynes with nitriles to give pyridines. The reaction can accommodate a very... 
ORGANIC-SYNTHESIS | CROSS-COUPLING REACTIONS | PYRIDINE-DERIVATIVES | EFFICIENT CATALYST | REGIOSELECTIVE CYCLOTRIMERIZATION | CO-CYCLIZATION | ALLYLIC ALKYLATION | TERMINAL ALKYNES | SELECTIVE SYNTHESIS | ACETYLENE CYCLOTRIMERIZATION | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2011, Volume 50, Issue 31, pp. 7162 - 7166
Joined by iron: The iron catalyst for the formation of pyridines at room temperature (see scheme), which was generated in situ from an inorganic iron salt and... 
iron | cycloaddition | nitriles | pyridines | heterocycles | ONE-STEP SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | METALATED PYRIDINES | 2 DIFFERENT ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | SUBSTITUTED PYRIDINES | REGIOSELECTIVE CYCLOTRIMERIZATION | TITANIUM(II) ALKOXIDE | COUPLING REACTIONS | INTRAMOLECULAR CYCLOTRIMERIZATION | CARBON-HETEROATOM
Journal Article