Asymmetric synthesis. XXXV1. Synthesis of 2-methyl 5-substituted substituted piperidines from chiral non-racemic lactams
✍ Scribed by Teresa Varea; Monique Dufour; Laurent Micouin; Claude Riche; Angèle Chiaroni; Jean-Charles Quirion; Henri-Philippe Husson
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 212 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Chiral a-amidophosphine boranes 7a-b can be diastereoselectively alkylated, using a phenylglycinol derivative as a chiral inducer, to furnish a-substituted a-amidophosphine boranes 8-12 with up to 99% diastereoisomeric excess. Selective reduction of the amidophosphine boranes afforded optically pure
## Abstract The reaction of substituted phenyl isocyanates with 2‐amino‐2‐phenylpropanenitrile and 2‐amino‐2‐(4‐nitrophenyl)propanenitrile has been used to prepare substituted 1‐(1‐cyanoethyl‐1‐phenyl)‐3‐phenylureas. In anhydrous phosphoric acid the first products to be formed from 1‐(1‐cyanoethyl‐