![Profiling the reactivity of cyclic C-nucleophiles towards electrophilic sulfur in cysteine sulfenic acid - Chemical Science (RSC Publishing) DOI:10.1039/C5SC02569A Profiling the reactivity of cyclic C-nucleophiles towards electrophilic sulfur in cysteine sulfenic acid - Chemical Science (RSC Publishing) DOI:10.1039/C5SC02569A](https://pubs.rsc.org/image/article/2016/SC/c5sc02569a/c5sc02569a-c4_hi-res.gif)
Profiling the reactivity of cyclic C-nucleophiles towards electrophilic sulfur in cysteine sulfenic acid - Chemical Science (RSC Publishing) DOI:10.1039/C5SC02569A
![Molecules | Free Full-Text | Transient Sulfenic Acids in the Synthesis of Biologically Relevant Products Molecules | Free Full-Text | Transient Sulfenic Acids in the Synthesis of Biologically Relevant Products](https://www.mdpi.com/molecules/molecules-23-01030/article_deploy/html/images/molecules-23-01030-sch004.png)
Molecules | Free Full-Text | Transient Sulfenic Acids in the Synthesis of Biologically Relevant Products
![Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediate | Scientific Reports Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediate | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep11870/MediaObjects/41598_2015_Article_BFsrep11870_Fig1_HTML.jpg)
Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediate | Scientific Reports
![a) A dipeptide-based sulfenic acid model. (b) Various 1,3-diketones... | Download Scientific Diagram a) A dipeptide-based sulfenic acid model. (b) Various 1,3-diketones... | Download Scientific Diagram](https://www.researchgate.net/publication/321835237/figure/fig9/AS:611938904051718@1522909012281/a-A-dipeptide-based-sulfenic-acid-model-b-Various-1-3-diketones-and-related.png)
a) A dipeptide-based sulfenic acid model. (b) Various 1,3-diketones... | Download Scientific Diagram
![Mining the Thiol Proteome for Sulfenic Acid Modifications Reveals New Targets for Oxidation in Cells | ACS Chemical Biology Mining the Thiol Proteome for Sulfenic Acid Modifications Reveals New Targets for Oxidation in Cells | ACS Chemical Biology](https://pubs.acs.org/cms/10.1021/cb900105q/asset/images/medium/cb-2009-00105q_0002.gif)
Mining the Thiol Proteome for Sulfenic Acid Modifications Reveals New Targets for Oxidation in Cells | ACS Chemical Biology
![Chemical proteomics reveals new targets of cysteine sulfinic acid reductase | Nature Chemical Biology Chemical proteomics reveals new targets of cysteine sulfinic acid reductase | Nature Chemical Biology](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41589-018-0116-2/MediaObjects/41589_2018_116_Fig1_HTML.png)
Chemical proteomics reveals new targets of cysteine sulfinic acid reductase | Nature Chemical Biology
![Cysteine sulfenic Acid as an Intermediate in Disulfide Bond Formation and Nonenzymatic Protein Folding | Biochemistry Cysteine sulfenic Acid as an Intermediate in Disulfide Bond Formation and Nonenzymatic Protein Folding | Biochemistry](https://pubs.acs.org/cms/10.1021/bi1008694/asset/images/medium/bi-2010-008694_0001.gif)
Cysteine sulfenic Acid as an Intermediate in Disulfide Bond Formation and Nonenzymatic Protein Folding | Biochemistry
![Reactivity, Selectivity, and Stability in Sulfenic Acid Detection: A Comparative Study of Nucleophilic and Electrophilic Probes | Bioconjugate Chemistry Reactivity, Selectivity, and Stability in Sulfenic Acid Detection: A Comparative Study of Nucleophilic and Electrophilic Probes | Bioconjugate Chemistry](https://pubs.acs.org/cms/10.1021/acs.bioconjchem.6b00181/asset/images/medium/bc-2016-00181f_0004.gif)