Metallated 2-alkenyl carbamates: chiral homoenolate reagents for asymmetric synthesis

Articles in the same Issue

1. Preface
2. Enzyme mimics
3. Synthetic methodology involving the carbopalladation of allenes
4. Stereocontrol in organic synthesis using silicon compounds
5. The psychobiological basis of heuristic synthesis planning - man, machine and the chiron approach
6. Mechanistic investigations of a biomimetic polycyclization process that leads to the Daphniphyllum alkaloids
7. CAMEO: a program for the logical prediction of the products of organic reactions
8. Synthetic applications of metallate rearrangements
9. Regio- and stereocontrolled catalytic palladium- and nickel 'ene-type' cyclizations
10. New synthetic methodology using organosulfur compounds
11. New perspectives of carbo- and hetero-l,3-dienes in organic synthesis
12. Synthesis of carbazole alkaloids
13. Synthetic routes proposed by a noninteractive synthesis program
14. Are flash pyrolytic reactions useful?
15. Sequential cross-coupling reactions as a versatile synthetic tool
16. Stereocontrol in allylboration reactions
17. Metallated 2-alkenyl carbamates: chiral homoenolate reagents for asymmetric synthesis
18. Methodology for stereochemical control in bioactive natural product synthesis - new methods toward enediyne antitumor antibiotics
19. Towards antibody-mediated metallo-porphyrin chemistry
20. α-silyl carbonyl compounds
21. Catalysis of organic reactions by inorganic solids
22. Stereoselective synthesis of inositol phosphates
23. Intramolecular alkoxy-carbonylation of hydroxy alkenes promoted by Pd(II)
24. Chiral building blocks based on technical grade β-citronellene
25. The directed ortho metalation reaction. Methodology, applications, synthetic links, and a non-aromatic ramification
26. Transition metal-stabilised vinylketenes
27. Stereo- and regioselective organic transformations based on main group organometallic reagents - application to the stereocontrolled Claisen rearrangements