Journal of the Chemical Society. Chemical communications p. 1085 - 1086 (1987)
Update date:2022-08-28
Topics:
Ranganathan, Subramania
Ranganathan, Darshan
Bhattacharyya, Dipti
The tryptophan side chain is transformed by in situ generated ruthenium(VIII), to that of aspartic acid, in good yields; amulti-step degradation sequence is suggested on the basis of the transformations of tetrahydrocarbazole to adipic acid, valine to isobutyric acid, and phenylalanine to phenylacetic acid.
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