Reductively-labile sulfonate ester protecting groups that are rapidly cleaved by physiological glutathione

Substrate Engineering Enabling Fluorescence Droplet Entrapment for IVC-FACS-Based Ultrahigh-Throughput Screening

(2016) Fuqiang Ma et al.   ANALYTICAL CHEMISTRY

Self-Immolative Spacers: Kinetic Aspects, Structure-Property Relationships, and Applications

(2015) Ahmed Alouane et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

TFA-promoted direct C–H sulfenylation at the C2 position of non-protected indoles

(2015) Thomas Hostier et al.   CHEMICAL COMMUNICATIONS

Synthesis of Aryl Sulfides: Metal-Free C–H Sulfenylation of Electron-Rich Arenes

(2015) Thomas Hostier et al.   ORGANIC LETTERS

Highly Enantioselective Organocatalytic α-Sulfenylation of Azlactones

(2014) Baokun Qiao et al.   ORGANIC LETTERS

Disulfide-Cleavage-Triggered Chemosensors and Their Biological Applications

(2013) Min Hee Lee et al.   CHEMICAL REVIEWS

A Trifluoroacetic Acid-labile Sulfonate Protecting Group and Its Use in the Synthesis of a Near-IR Fluorophore

(2012) Steven M. Pauff et al.   JOURNAL OF ORGANIC CHEMISTRY

Design and application of esterase-labile sulfonate protecting groups

(2011) Laert Rusha et al.   CHEMICAL COMMUNICATIONS

Synthesis of Near-IR Fluorescent Oxazine Dyes with Esterase-Labile Sulfonate Esters

(2011) Steven M. Pauff et al.   ORGANIC LETTERS

Profiling Sulfonate Ester Stability: Identification of Complementary Protecting Groups for Sulfonates

(2010) Stephen C. Miller   JOURNAL OF ORGANIC CHEMISTRY

Trichloroethyl Group As a Protecting Group for Sulfonates and Its Application to the Synthesis of a Disulfonate Analog of the Tyrosine Sulfated PSGL-143−50Peptide

(2009) Ahmed M. Ali et al.   JOURNAL OF ORGANIC CHEMISTRY