Abstract
Natural L-homocysteine and L,L-cystathionine,
along with a series of unnatural analogues, have been
prepared from L-aspartic and L-glutamic acid. Manipulation
of the protected derivatives provided x-iodoamino acids,
which were used in thioalkylation reactions of sulfur
nucleophiles, such as the ester of L-cysteine and potassium
thioacetate.
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