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Time-resolved detection of SDS-induced conformational changes in α-synuclein by a micro-stopped-flow system. Shunki Takaramoto, Yusuke Nakasone, Kei Sadakane, Shinsaku Maruta, Masahide Terazima , RSC Adv. , 2021 , 11 , 1086

A combination of experiment and theoretical methods to study the novel and low-cost corrosion inhibitor 1-hydroxy-7-azabenzotriazole for mild steel in 1 M sulfuric acid. Lanzhou Gao, Shini Peng, Zhili Gong, Jie Chen , RSC Adv. , 2018 , 8 , 38506

Novel acylation catalysts in peptide synthesis: derivatives of N-hydroxytriazoles and N-hydroxytetrazoles. Jane C. Spetzler, Morten Meldal, Jakob Felding, Per Vedsø, Mikael Begtrup , J. Chem. Soc., Perkin Trans. 1 , 1998 , 1727

A chemoselective α-aminoxylation of aryl ketones: a cross dehydrogenative coupling reaction catalysed by Bu4NI. Yogesh Siddaraju, Kandikere Ramaiah Prabhu , Org. Biomol. Chem. , 2015 , 13 , 11651

Full solid-phase total synthesis of macrocyclic natural peptides using four-dimensionally orthogonal protective groups. Hiroaki Itoh, Masayuki Inoue , Org. Biomol. Chem. , 2019 , 17 , 6519

Amide bond formation: beyond the myth of coupling reagents. Eric Valeur, Mark Bradley , Chem. Soc. Rev. , 2009 , 38 , 606

Oxyma-B, an excellent racemization suppressor for peptide synthesis. Yahya E. Jad, Sherine N. Khattab, Beatriz G. de la Torre, Thavendran Govender, Hendrik G. Kruger, Ayman El-Faham, Fernando Albericio , Org. Biomol. Chem. , 2014 , 12 , 8379

Solid-phase synthesis of protected α-amino phosphonic acid oligomers. Yoshitaka Ishibashi, Masato Kitamura , Chem. Commun. , 2009 , 6985

Advantageous applications of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesis. Louis A. Carpino, Ayman El-Faham, Charles A. Minor, Fernando Albericio , J. Chem. Soc., Chem. Commun. , 1994 , 201

Amino acid fluorides: viable tools for synthesis of peptides, peptidomimetics and enantiopure heterocycles. Girish Prabhu, N. Narendra, Basavaprabhu, V. Panduranga, Vommina V. Sureshbabu , RSC Adv. , 2015 , 5 , 48331