Electrochemical Deprotection of Amino Groups: Advancing Sustainable Peptide Synthesis (#224)
Esteban Suárez-Picado
1
,
Lara R. Malins
1
- Research School of Chemistry, The Australian National University, and Australian Research Council Centre of Excellence for Innovations in Peptide and Protein Science, Acton, ACT, Australia
Publish consent withheld
- (1) (a) de la Torre, B. G.; Albericio, F. Peptide Therapeutics 2.0. Molecules 2020, 25 (10), 2293. (b) Wang, L.; Wang, N.; Zhang, W.; Cheng, X.; Yan,
Z.; Shao, G.; Wang, X.; Wang, R.; Fu, C. Therapeutic Peptides: Current Applications and Future Directions. Signal Transduct. Target. Ther.
2022, 7 (1), 48.
- (2) Barnhurst, L. A.; Wan, Y.; Kutateladze, A. G. Efficient Electrochemical Deprotection of Carboxylic and Amino Acids from Their 2-
(Hydroxymethyl)-1,3-Dithiane (Dim) Esters. Org. Lett. 2000, 2 (6), 799–801.
- (3) Manuscript submitted.