ChemInform Abstract: A Multicomponent Formal [1 + 2 + 1 + 2]-Cycloaddition for the Synthesis of Dihydropyridines.
β Scribed by P. Ricardo Girling; Andrei S. Batsanov; Hong C. Shen; Andrew Whiting
- Book ID
- 115552216
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 35 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
1999 pyridine derivatives with bridges pyridine
Formal [4 + 2] Intramolecular Ketenimine-Imine Cycloaddition. Synthesis of Benzimidazo[1,2-b]isoquinolines. -Formal [4+2] cycloaddition of ketenimine intermediates (V) derived from the azides (III) and diphenylketene (IV) by aza-Wittig reaction, provides the partially saturated compounds (VI). They
A New [4 + 2] Cycloaddition Strategy for the Synthesis of N-Acyl-7-azabicyclo[2.2.1]heptan-2-ones: A Formal Synthesis of (Β±)-Epibatidine. -The title compound (VIII), an intermediate for the preparation of (Β±)-epibatidine, is prepared via Diels-Alder reaction of allenes with N-acylated pyrrole (II)