Rigid aminoalcohol backbone as a highly defined chiral template for the preparation of optically active tertiary α-hydroxyl acids

✍ Scribed by Chris H. Senanayake; Kevin Fang; Paul Grover; Roger P. Bakale; Charles P. Vandenbossche; Stephen A. Wald

• Book ID: 104260552
• Publisher: Elsevier Science
• Year: 1999
• Tongue: French
• Weight: 279 KB
• Volume: 40
• Category: Article
• ISSN: 0040-4039
• DOI: 10.1016/s0040-4039(98)02587-8

✦ Synopsis

Constrained aminoalcohol derived-ketoester or amides have provided a new enttT ]or the production of enantiopure acid l for (S)-oxybutynin.