Advances in Fmoc solid‐phase peptide synthesis
R Behrendt, P White, J Offer - Journal of Peptide Science, 2016 - Wiley Online Library
Today, Fmoc SPPS is the method of choice for peptide synthesis. Very‐high‐quality Fmoc
building blocks are available at low cost because of the economies of scale arising from …
building blocks are available at low cost because of the economies of scale arising from …
The road to the synthesis of “difficult peptides”
M Paradís-Bas, J Tulla-Puche, F Albericio - Chemical Society Reviews, 2016 - pubs.rsc.org
The last decade has witnessed a renaissance of peptides as drugs. This progress, together
with advances in the structural behavior of peptides, has attracted the interest of the …
with advances in the structural behavior of peptides, has attracted the interest of the …
Recent advances in chemical protein synthesis: method developments and biological applications
S Dong, JS Zheng, Y Li, H Wang, G Chen… - Science China …, 2024 - Springer
The central dogma of modern biology underscores the pivotal roles proteins play in diverse
biological processes, the study of which necessitates advanced methods to produce …
biological processes, the study of which necessitates advanced methods to produce …
Site-selective modification of peptide backbones
A Boto, CC González, D Hernández… - Organic Chemistry …, 2021 - pubs.rsc.org
The site-selective modification of peptide backbones allows an outstanding fine-tuning of
peptide conformation, folding ability, and physico-chemical and biological properties …
peptide conformation, folding ability, and physico-chemical and biological properties …
Synthesis of l‐ and d‐Ubiquitin by One‐Pot Ligation and Metal‐Free Desulfurization
YC Huang, CC Chen, S Gao, YH Wang… - … A European Journal, 2016 - Wiley Online Library
Native chemical ligation combined with desulfurization has become a powerful strategy for
the chemical synthesis of proteins. Here we describe the use of a new thiol additive, methyl …
the chemical synthesis of proteins. Here we describe the use of a new thiol additive, methyl …
Design, synthesis, and utility of defined molecular scaffolds
A growing theme in chemistry is the joining of multiple organic molecular building blocks to
create functional molecules. Diverse derivatizable structures—here termed “scaffolds” …
create functional molecules. Diverse derivatizable structures—here termed “scaffolds” …
Total chemical synthesis of a thermostable enzyme capable of polymerase chain reaction
Polymerase chain reaction (PCR) has been a defining tool in modern biology. Towards
realizing mirror-image PCR, we have designed and chemically synthesized a mutant …
realizing mirror-image PCR, we have designed and chemically synthesized a mutant …
Resonance assisted hydrogen bonding phenomenon unveiled through both experiments and theory: a new family of ethyl N‐salicylideneglycinate dyes
DS Shapenova, AA Shiryaev, M Bolte… - … A European Journal, 2020 - Wiley Online Library
Extensive experimental and theoretical investigations are reported on the nature of
resonance‐assisted hydrogen bonding phenomenon (RAHB) and its influence on …
resonance‐assisted hydrogen bonding phenomenon (RAHB) and its influence on …
DIC/Oxyma‐based accelerated synthesis and oxidative folding studies of centipede toxin RhTx
XT Chen, JY Wang, YN Ma, LY Dong… - Journal of Peptide …, 2022 - Wiley Online Library
Coupling reagents play crucial roles in the iterative construction of amide bonds for the
synthesis of peptides and peptide‐based derivatives. The novel DIC/Oxyma condensation …
synthesis of peptides and peptide‐based derivatives. The novel DIC/Oxyma condensation …
A backbone amide protecting group for overcoming difficult sequences and suppressing aspartimide formation
ABM Abdel‐Aal, G Papageorgiou, R Raz… - Journal of Peptide …, 2016 - Wiley Online Library
A backbone amide bond protecting group, 2‐hydroxy‐4‐methoxy‐5‐nitrobenzyl (Hmnb),
improved the synthesis of aggregation and aspartimide‐prone peptides. Introduction of …
improved the synthesis of aggregation and aspartimide‐prone peptides. Introduction of …