Development of a new amino-protecting group, 2-adamantyloxycarbonyl (2-adoc), and its application to the solid-phase synthesis of protected peptides
Yasuhiro Nishiyama, Yoshio Okada
Abstract
Yasuhiro Nishiyama, Yoshio Okada
Abstract
A new ε-amino protecting group, 2-adamantyloxycarbonyl (2-Adoc) has been developed, and its application to the solid phase synthesis of the protected peptide has been demonstrated successfully in combination with Nα-fluoren-9-ylmethoxycarbonyl (Fmoc) protection and trifluoroacetic acid (TFA)-cleavable resin support.
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A new ε-amino protecting group, 2-adamantyloxycarbonyl (2-Adoc) has been developed, and its application to the solid phase synthesis of the protected peptide has been demonstrated successfully in combination with Nα-fluoren-9-ylmethoxycarbonyl (Fmoc) protection and trifluoroacetic acid (TFA)-cleavable resin support.
Key concepts: Trifluoroacetic acid, Protecting group, Solid-phase synthesis, Chemistry, Peptide synthesis, Peptide, Combinatorial chemistry, Amino acid