Development of an efficient synthetic strategy for bioactive alkaloids possessing a spirocyclic ring system

Articles in the same Issue

1. Preface
2. Lessons from the total synthesis of (±)-phalarine: Insights into the mechanism of the Pictet–Spengler reaction
3. Use of functionalized β-lactams as building blocks in heterocyclic chemistry
4. Proximity-assisted cycloaddition reactions of ω-azido cyanohydrin ethers: Synthesis of diversely functionalized bicyclic tetrazoles
5. Development of an efficient synthetic strategy for bioactive alkaloids possessing a spirocyclic ring system
6. Recent chemoenzymatic total syntheses of natural and unnatural products: Codeine, balanol, pancratistatin, and oseltamivir
7. Intramolecular annulations of donor–acceptor cyclopropanes
8. Synthesis of axially chiral bipyridine N,N'-dioxides and enantioselective allylation of aldehydes
9. Copper-catalyzed enantioselective aziridination of styrenes
10. Synthesis of heterocycles via alkoxyallenes
11. Enantioselective reactions catalyzed by chiral pyridine 2,6-bis(5',5'-diphenyloxazoline)-metal complexes