Publications
Chemical Protein Synthesis via Direction-Switching One-Pot Peptide Ligation Enabled by Orthogonal Cysteinyl Protection
J Am Chem Soc
(2026)
148
4622
(doi: 10.1021/jacs.5c20510)
Chemical protein synthesis via one-pot multiple peptide ligation strategies
(2024)
1
One-pot ligation of multiple peptide segments via N-terminal thiazolidine deprotection chemistry.
(2024)
698
169
(doi: 10.1016/bs.mie.2024.04.020)
Repetitive Thiazolidine Deprotection Using a Thioester‐Compatible Aldehyde Scavenger for One‐Pot Multiple Peptide Ligation**
Angewandte Chemie (International ed. in English)
(2022)
61
e202206240
(doi: 10.1002/anie.202206240)
Fmoc-Compatible and C-terminal-Sequence-Independent Peptide Alkyl Thioester Formation Using Cysteinylprolyl Imide.
Organic letters
(2020)
22
4670
(doi: 10.1021/acs.orglett.0c01450)
Toolbox for chemically synthesized histone proteins.
Current Opinion in Chemical Biology
(2020)
58
10
(doi: 10.1016/j.cbpa.2020.04.016)
Cysteinylprolyl imide (CPI) peptide: a highly reactive and easily accessible crypto-thioester for chemical protein synthesis.
Chemical science
(2019)
10
5967
(doi: 10.1039/c9sc00646j)
