Related references
Note: Only part of the references are listed.Site-specific functionalisation of proteins by a Staudinger-type reaction using unsymmetrical phosphites
Verena Boehrsch et al.
CHEMICAL COMMUNICATIONS (2010)
Solid-Phase Synthesis of Phosphoramidate-Linked Glycopeptides
Da'san M. M. Jaradat et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2010)
Site-specific PEGylation of proteins by a Staudinger-phosphite reaction
Remigiusz Serwa et al.
CHEMICAL SCIENCE (2010)
Chemoselective Staudinger-Phosphite Reaction of Azides for the Phosphorylation of Proteins
Remigiusz Serwa et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2009)
Asymmetric bronsted acid catalysis: Enantioselective nucleophilic substitutions and 1,4-additions
Magnus Rueping et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Enantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl ether: The difference between bronsted and Lewis acid catalysis
Peng Jiao et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Lewis base catalysis in organic synthesis
Scott E. Denmark et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Synthesis of and evaluation of lipid A modification by 4-substituted 4-deoxy arabinose analogs as potential inhibitors of bacterial polymyxin resistance
T. Kline et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2008)
Design of chiral N-triflyl phosphoramide as a strong chiral Bronsted acid and its application to asymmetric Diels-Alder reaction
Daisuke Nakashima et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)
Organic azides: An exploding diversity of a unique class of compounds
S Brase et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2005)
Phosphinic peptides: Synthetic approaches and biochemical evaluation as Zn-metalloprotease inhibitors
A Yiotakis et al.
CURRENT ORGANIC CHEMISTRY (2004)
Hydrolysis of the phosphonamidate bond in phosphono dipeptide analogues - The influence of the nature of the N-terminal functional group
A Mucha et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2003)
Synthesis of the first stable phosphonamide transition state analogue
P de Medina et al.
JOURNAL OF ORGANIC CHEMISTRY (2003)
The most potent organophosphorus inhibitors of leucine aminopeptidase. Structure-based design, chemistry, and activity
J Grembecka et al.
JOURNAL OF MEDICINAL CHEMISTRY (2003)
Share Paper
