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Methylthiomethylation and subsequent sulfoxidation and pyrolysis of the N-Boc-protected ß3-amino acid methyl esters derived from Ala, Val, and Leu provided the a-methylene esters; these were then used to synthesize the ß-peptides specified in the title (step-by-step and fragment coupling in solution). The novel ß-peptides were fully characterized, but neither solid-state nor solution structures were found.
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Bierbaum et al. (2004) studied this question.
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