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Cited by in F6Publishing
For: He R, Pan J, Mayer JP, Liu F. Stepwise Construction of Disulfides in Peptides. Chembiochem 2020;21:1101-11. [PMID: 31886929 DOI: 10.1002/cbic.201900717] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Laps S, Atamleh F, Kamnesky G, Uzi S, Meijler MM, Brik A. Insight on the Order of Regioselective Ultrafast Formation of Disulfide Bonds in (Antimicrobial) Peptides and Miniproteins. Angew Chem Int Ed Engl 2021;60:24137-43. [PMID: 34524726 DOI: 10.1002/anie.202107861] [Reference Citation Analysis]
2 Laps S, Atamleh F, Kamnesky G, Sun H, Brik A. General synthetic strategy for regioselective ultrafast formation of disulfide bonds in peptides and proteins. Nat Commun 2021;12:870. [PMID: 33558523 DOI: 10.1038/s41467-021-21209-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
3 Ma D, Sun J, Shen S, Chen H, Xu W, Wang Y, Song C, Shi T, Huo S. Deprotection of S-Acetamidomethyl and 1,3-Thiazolidine-4-Carbonyl Protecting Groups from Cysteine Side Chains in Peptides by trans-[PtX2(CN)4]2-: One-Pot Regioselective Synthesis of Disulfide Bonds. J Org Chem 2022;87:1470-6. [PMID: 34985274 DOI: 10.1021/acs.joc.1c02793] [Reference Citation Analysis]
4 Fährmann J, Hilt G. Electrochemical Synthesis of Organic Polysulfides from Disulfides by Sulfur Insertion from S8 and an Unexpected Solvent Effect on the Product Distribution. Chemistry 2021;27:11141-9. [PMID: 33938070 DOI: 10.1002/chem.202101023] [Reference Citation Analysis]
5 Spears RJ, McMahon C, Shamsabadi M, Bahou C, Thanasi IA, Rochet LNC, Forte N, Thoreau F, Baker JR, Chudasama V. A novel thiol-labile cysteine protecting group for peptide synthesis based on a pyridazinedione (PD) scaffold. Chem Commun (Camb) 2021. [PMID: 34747956 DOI: 10.1039/d1cc03802h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Spears RJ, McMahon C, Chudasama V. Cysteine protecting groups: applications in peptide and protein science. Chem Soc Rev 2021;50:11098-155. [PMID: 34605832 DOI: 10.1039/d1cs00271f] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
7 Chakraborty A, Sharma A, Albericio F, de la Torre BG. Disulfide-Based Protecting Groups for the Cysteine Side Chain. Org Lett 2020;22:9644-7. [PMID: 33232171 DOI: 10.1021/acs.orglett.0c03705] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Wang Y, Xing Y, Sun J, Song C, Shen S, Huo S. Polymer Supported Methionine Selenoxide as an Excellent Immobilized Oxidant for the Formation of Disulfide Bonds in Peptides. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201361] [Reference Citation Analysis]