Cobalt-mediated cyclotrimerization and cycloisomerization reactions. Synthetic applications

Articles in the same Issue

1. Recent advances in selective organic synthesis mediated by transition metal complexes
2. Olefin metathesis–recent applications in synthesis
3. The application of ligands with planar chirality in asymmetric synthesis
4. Chiral copper (ii) complexes as Lewis acids for catalyzed cycloaddition, carbonyl addition, and conjugate addition reactions
5. Approaches to catalyst discovery. New carbon–heteroatom and carbon–carbon bond formation
6. Transition metal catalysis in organic synthesis: reflections, chirality and new vistas
7. Palladium-catalyzed annulation
8. The bite angle makes the catalyst
9. Chiral nitrogen-stabilized Fischer carbene complexes: an efficient tool in the stereocontrolled elaboration of additional stereogenic centers
10. Cobalt-mediated cyclotrimerization and cycloisomerization reactions. Synthetic applications
11. Ring-opening polymerization of strained metallocenophanes: a new route to high molecular weight poly(metallocenes)
12. Selectivity and reactivity in asymmetric allylic alkylation
13. Organometallic chemistry directed towards the synthesis of electroactive materials: stereoselective routes to extended polyconjugated systems
14. Rapid, productive and stereoselective hydrogenation of ketones
15. Strategies for the development of enantioselective catalysts
16. Bicyclization of dienes, enynes, and diynes with Ti(ii) reagent. New developments towards asymmetric synthesis
17. The directed ortho metalation–transition metal–catalyzed reaction symbiosis in heteroaromatic synthesis
18. Recent studies in asymmetric catalysis using ferrocenyl ligands
19. Recollections of organopalladium chemistry
20. An Extension to the JCAMP-DX Standard File Format, JCAMP-DX V.5.01
21. Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)
22. Guidelines for the use of the Internet by IUPAC bodies
23. Atomic Weights of the Elements 1997
24. Substituent effects on the O-H bond dissociation enthalpies in phenolic compounds: agreements and controversies