STRUCTURAL AND STEREOCHEMICAL STUDIES OF METHIONINE DECARBOXYLASE FROM DRYOPTERIS FELIX-MAS

DOI: 10.1016/S0040-4039(00)85294-6

Source and publish data:

Tetrahedron Letters p. 5661 - 5664 (1986)

Update date:2022-07-30

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Authors:

Stevenson, David E.

Akhtar, Mahmoud

Gani, David

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Article abstract of DOI:10.1016/S0040-4039(00)85294-6

Each diastereomer of N-(-)-camphanoyl-(3-methylthio)-1-aminopropane chirally deuteriated at C-1 has been synthesized and compared to deuteriated samples derived from L-methionine via enzymic decarboxylation.Here we report that decarboxylation occurs in a retentive mode.

Full text of DOI:10.1016/S0040-4039(00)85294-6

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