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

Chris H Senanayake, Kevin Fang + Show 4 more

https://doi.org/10.1016/s0040-4039(98)02587-8

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Journal: Tetrahedron Letters	Publication Date: Jan 1, 1999
Citations: 64

Abstract

Constrained aminoalcohol derived-ketoester or amides have provided a new entry for the production of enantiopure acid 1 for (S)-oxybutynin.

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