## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A Straightforward Entry to 7-Azabicyclo[2.2.1]heptane-1-carbonitriles in the Synthesis of Novel Epibatidine Analogues
β Scribed by Thomas Heugebaert; Joke Van Hevele; Wouter Couck; Vicky Bruggeman; Sarah Van der Jeught; Kurt Masschelein; Christian V. Stevens
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 179 KB
- Volume
- 2010
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
New Synthesis of 7-(tert-Butoxycarbonyl)-7-azabicyclo[2.2.1]hept-2-ene. A Key Intermediate in the Synthesis of Epibatidine and Analogues. -In continuation of efforts on efficient synthetic routes to the alkaloid epibatidine (V), an improved procedure for the synthesis of the N-Boc protected azabicy
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)