A novel strategy for the synthesis of 2-arylpyridines using one-pot 6π-azaelectrocyclization
✍ Scribed by Toyoharu Kobayashi; Sho Hatano; Hiroshi Tsuchikawa; Shigeo Katsumura
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 272 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Summarv: A novel and efficient synthesis of 2,6-dideoxy-a-glycosides was developed by use of phenyl 2,6-anhydro-1,2-dithio-D-altropyranosides as glycosyl donors in a highly stereocontrolled glycosyla tion . Highly stereocontrolled synthesis of 2,6-dideoxy glycosides is of considerable interest
A novel and efficient protocol is developed for the synthesis of various spiro-2-amino pyrimidinones via the three-component condensation of alkyl cyanoacetates, guanidinium carbonate and N-substituted 4-piperidinones in ethanol at reflux. High yields, neutral conditions, and short reaction times ar
A simple, time-saving, and user-friendly one-pot strategy is demonstrated for the synthesis of a novel ternary reduced graphite oxide/SnO 2 /Au hybrid nanomaterials using exfoliated graphite oxide, SnCl 2 and HAuCl 4 as the staring materials. The synthesis process can be finished within 2 h in a sol
## Abstract magnified image A variety of 2‐aryl quinazolines were synthesized from the condensation of 2‐aminobenzylamines and aryl aldehydes to form 2‐aryl‐1,2,3,4‐tetrahydroquinazolines and subsequent oxidation of the intermediates with MnO~2~. J. Heterocyclic Chem., (2010).