Evaluation of acid-labileS-protecting groups to prevent Cys racemization in Fmoc solid-phase peptide synthesis

Microwave Heating in the Solid-Phase Synthesis ofN-Methylated Peptides: When Is Room Temperature Better?

(2012) Renée Roodbeen et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Synthesis and application ofNα-Fmoc-Nπ-4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis

(2012) Hajime Hibino et al.   JOURNAL OF PEPTIDE SCIENCE

4-Methoxybenzyloxymethyl Group, a Racemization-Resistant Protecting Group for Cysteine in Fmoc Solid Phase Peptide Synthesis

(2012) Hajime Hibino et al.   ORGANIC LETTERS

Acid-Labile Cys-Protecting Groups for the Fmoc/tBu Strategy: Filling the Gap

(2012) Miriam Góngora-Benítez et al.   ORGANIC LETTERS

4-Methoxybenzyloxymethyl group as an Nπ-protecting group for histidine to eliminate side-chain-induced racemization in the Fmoc strategy

(2011) Hajime Hibino et al.   TETRAHEDRON LETTERS

Amino Acid-Protecting Groups

(2009) Albert Isidro-Llobet et al.   CHEMICAL REVIEWS

Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]

(2009) Ramon Subirós-Funosas et al.   CHEMISTRY-A EUROPEAN JOURNAL