A direct method for the synthesis of orthogonally protected furyl- and thienyl- amino acids
Tóm tắt
The synthesis of unnatural amino acids plays a key part in expanding the potential application of peptide-based drugs and in the total synthesis of peptide natural products. Herein, we report a direct method for the synthesis of orthogonally protected 5-membered heteroaromatic amino acids.
Tài liệu tham khảo
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