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trans-4-Hydroxy-L-proline is used as a reagent for the preparation of neuroexcitatory kainoids and antifungal echinocandins. It is also involved in the synthesis of chiral ligands for enantioselective ethylation of aldehydes.
Chiral precursor for a wide variety of synthetic targets. For discussion of some examples, see: Tetrahedron, 52, 13803 (1996).
Satomura, T.; Ishikura, M.; Koyanagi, T.; Sakuraba, H.; Ohshima, T.; Suye, S. I. Dye-linked d-amino acid dehydrogenase from the thermophilic bacterium Rhodothermus marinus JCM9785: characteristics and role in trans-4-hydroxy-l-proline catabolism. Appl. Microbiol. Biotechnol. 2015, 99 (10), 4265-4275.
Kuttan, R.; Panikkar, B.; Binitha, P. P. Amino acids in sandal (Santalum album L) with special reference to cis-4-hydroxy-l-proline and sym. homospermidine. Springerplus 2015, 4 (1), 1-9.