Amino acids, XII: (±)Pipecolic acid derivatives - Part 2: An expedient synthetic entry to substituted pipecolic acids

DOI: 10.1002/ardp.19923250709

Source and publish data:

Archiv der Pharmazie p. 419 - 423 (1992)

Update date:2022-07-29

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Authors:

Herdeis Herdeis

Engel Engel

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Article abstract of DOI:10.1002/ardp.19923250709

The Diels-Alder product 1 is transformed by Noyori reaction and catalytic hydrogenation to 4. Hydrolysis with concomitant decarboxylation of 4 furnishes the trans configuration amino acid 5. Functional group transformation (reduction, lactonization) of 5

Full text of DOI:10.1002/ardp.19923250709

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