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Fluorescently labeled inhibitor for profiling cytoplasmic peptide:N-glycanase.
Results suggest that BODIPY-(GlcNAc)(2)-ClAc could be an in vivo inhibitor of cytoplasmic PNGase.
Trifluoromethylation reactions for the synthesis of β-trifluoromethylamines.
A multitalented system: N-migratory oxytrifluoromethylation and one-pot three-component reactions of allylamines as well as the aminotrifluoromethylation of alkenyl amines all proceeded efficiently
A New Enantioselective Total Synthesis of AI-77-B
An enantioselective total synthesis of AI-77-B (1), a gastroprotective substance isolated from a culture broth of Bacillus pumilus AI-77, was performed in high overall yield. In this synthesis, the
A "catch-and-release" protocol for alkyne-tagged molecules based on a resin-bound cobalt complex for peptide enrichment in aqueous media.
Selective enrichment and detection of an amine derived from the "catch and release" of an alkyne-tagged dipeptide in the presence of various peptides has been accomplished under highly dilute conditions, as determined by mass spectrometry.
Systematic synthesis and inhibitory activity of haloacetamidyl oligosaccharide derivatives toward cytoplasmic peptide:N-glycanase
The results underscore the importance of the N-acetyl groups of chitobiose for PNGase recognition, and reactivity and position of the leaving group at the reducing end are also important factors.
A study of (binap)(enyne)tetracarbonyldicobalt(0) complexes.
Four (binap)(enyne)tetracarbonyldicobalt(0) complexes have been synthesised and their reactivity monitored by variable temperature NMR spectroscopy, and the structure of 12 was determined by X-ray crystallography, and its presence under Pauson-Khand reaction conditions was verified by NMRSpectroscopy.
A New Enantioselective Synthesis of the Aminodihydroisocoumarin Moiety of AI-77-B
The aminodihydroisocoumarin moiety of AI-77-B, a gastroprotective substance isolated from Bacillus pumilus AI-77, has been prepared from a convenient chiral synthon of L-erythrose by combination of