Tetrahedron Letters p. 5661 - 5664 (1986)
Update date:2022-07-30
Topics:
Stevenson, David E.
Akhtar, Mahmoud
Gani, David
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.
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