The use of kinetically generated unstable enolate ions in the regiospecific formation of carbonxarbon bonds. Specific applications to annelation processes

Articles in the same Issue

1. Opening remarks
2. The cyclopropanation of silyl enol ethers. A powerful synthetic tool
3. Chiral recognition in complexation of guests by designed host molecules
4. The importance of conformation of the tetrahedral intermediate in the hydrolysis of esters and amides
5. The effect of pressure on the electronic states of organic solids
6. Asymmetric catalysis by chiral rhodium complexes in hydrogenation and hydrosilylation reactions
7. Synthetic studies in the field of natural products
8. Two-phase reactions in the chemistry of carbanions and halocarbenes. A useful tool in organic synthesis
9. Applications of thallium(III) nitrate (TTN) to organic synthesis
10. Singlet oxygen: a reagent in organic synthesis
11. The use of polymeric reagents in organic synthesis
12. Industrial synthesis of terpene compounds
13. The use of kinetically generated unstable enolate ions in the regiospecific formation of carbonxarbon bonds. Specific applications to annelation processes
14. Novel approaches to alkylations