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

DOI: 10.1016/S0040-4039(98)02587-8

Source and publish data:

Tetrahedron Letters p. 819 - 822 (1999)

Update date:2022-07-31

Topics:

Authors:

Senanayake, Chris H.

Fang, Kevin

Grover, Paul

Bakale, Roger P.

Vandenbossche, Charles P.

Wald, Stephen A.

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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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