Demonstrates high enantioselectivity in alkylation for unnatural amino acids, indicating its robust utility in synthesis.
) bond formation. While deamination strategies are well explored, asymmetric variants remain underdeveloped. This methodology addresses that gap, delivering high enantioselectivity across a broad substrate scope, including natural product-derived and conformationally constrained scaffolds. The protocol is further applied to the synthesis of unnatural amino acid analogues and polypeptides without a loss of enantiopurity, demonstrating its utility and robustness in asymmetric synthesis.
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Singh et al. (2026) studied this question.
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