Synthesis of Indole Derivatives via Isocyanides
✍ Scribed by J. Campo; M. Garcia-Valverde; S. Marcaccini; M. J. Rojo; T. Torroba
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 8 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The intramolecular Knoevenagel condensation of __N__‐cyclohexyl 3‐aryl‐2‐(2‐nitrophenyl)acetoxy‐3‐oxopropionamides 4 obtained from 2‐nitrophenylacetic acid (1), arylglyoxals 2 and cyclohexyl isocyanide (3) afforded __N__‐cyclohexyl 3‐aryl‐2,5‐dihydro‐2‐(2‐nitrophenyl)‐5‐oxofuran‐2‐carbo
## Abstract magnified image A series of new carbazolo[2,1‐__a__]carbazoles was synthesized from 4‐oxo‐1,2,3,4‐tetrahydrobenzo[__a__]‐carbazole derivatives.
## Abstract The reaction between arylglyoxals (1), cyclohexyl isocyanide, and aromatic carboxylic acids (2) affords __N__‐cyclohexyl‐2‐acyloxy‐3‐aryl‐3‐oxopropionic amides (3) which can be cyclized to __N__‐cyclohexyl‐2,4‐diaryl‐5‐oxazolecarboxamides (4).