Amanote Research
Register
Sign In
Rapid, Stoichiometric, Site-Specific Modification of Aldehyde-Containing Proteins Using a Tandem Knoevenagel-Intra Michael Addition Reaction
doi 10.1021/acs.bioconjchem.8b00086.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Stereoselective Synthesis of Indanylglycine Derivatives by a Tandem Michael–Michael Reaction
Synlett
Organic Chemistry
Site-Specific Incorporation of a Dithiolane Containing Amino Acid Into Proteins
Synthesis of 2,3,4-Trisubstituted Thiochromanes Using an Organocatalytic Enantioselective Tandem Michael-Henry Reaction
Advanced Synthesis and Catalysis
Organic Chemistry
Catalysis
Selective Lysine Modification of Native Peptides via Aza-Michael Addition
Organic and Biomolecular Chemistry
Organic Chemistry
Theoretical Chemistry
Biochemistry
Physical
Modification of Aniline Containing Proteins Using an Oxidative Coupling Strategy
The Michael Reaction. Mechanism, Stereochemistry and a Synthetically Useful Modification.
Acta Chemica Scandinavica
Rapid Modification of Proteins Using a Rapamycin-Inducible Tobacco Etch Virus Protease System
PLoS ONE
Multidisciplinary
Domino Reaction of Pyrrolidinium Ylides: Michael Addition/[1,2]-Stevens Rearrangement
Rapid Addition of Unlabeled Silent Solubility Tags to Proteins Using a New Substrate-Fused Sortase Reagent
Journal of Biomolecular NMR
Biochemistry
Spectroscopy
