General Characteristics The Eschenmoser coupling begins with the S-alkylation of thioamides and gives enamine products (vinylogous amides, urethanes, etc.). As shown below, thiophiles (e.g. ...
- Chemoinformatically Guided Discovery of Chiral Catalysts...
- Process Mass Intensity, PMI...
- Cell-Permeant Large Stokes Shift Dyes for Transfection-Free Multicolor Nanoscopy...
- Complex Acid Chlorides from Unsaturated Hydrocarbons...
- Ugi Reaction for Alternating Peptides...
- Arylation at Lysine Residues...
- Near-Infrared Light Activated Azo-BF2 Switches...
- An Excimer-Based, Turn-On Fluorescent Sensor for the Selective Detection of Diphosphorylated Protein...
- Small-Molecule Labeling of Live Cell Surfaces for Three-Dimensional Super-Resolution Microscopy...
- Photoelectric Signal Conversion by Combination of Electron-Transfer Chain Catalytic Isomerization an...
- Lighting Up Individual DNA Damage Sites by In Vitro Repair Synthesis...
- Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Bas...
- Dual Changes in Conformation and Optical Properties of Fluorophores within a Metal−Organic Framework...
- Far-Red Fluorescence Probe for Monitoring Singlet Oxygen during Photodynamic Therapy...
- Accessing Zinc Monohydride Cations through Coordinative Interactions...
- Arylazopyrazoles: Azoheteroarene Photoswitches Offering Quantitative Isomerization and Long Thermal ...
- Quantitative Photoswitching in Bis(dithiazole)ethene Enables Modulation of Light for Encoding Optica...
- A Mitochondria-Targetable Fluorescent Probe for Dual-Channel NO Imaging Assisted by Intracellular Cy...
- Modulating Short Wavelength Fluorescence with Long Wavelength Light...
- Reversible Photochromic System Based on Rhodamine B Salicylaldehyde Hydrazone Metal Complex...