Herein, we report a new class of glycosyl donors, benzoxazolyl imidates, for chemical glycosylation. The O-benzoxazolyl (OBox) leaving group was designed with an aim to compare the relative reactivity and stability of similarly structured S-benzoxazolyl (SBox) glycosides (thioimidates) developed in our lab and glycosyl trichloroacetimidates (TCAI, O-imidates) developed by Schmidt. Novel OBox do...

Intramolecular hydroxyl attack upon iron-coordinated nitriles in a {closo-2,1,10-FeC2B7} system forms imidates that allow construction of a tetra-cluster {FeC2B7}-{C2Co2}-{C2Co2}-{FeC2B7} molecule.

The application of [4+2] cycloadditions between alkenes and an N-benzoyl iminium species, generated in situ under acidic conditions, is described in the synthesis of diverse molecular scaffolds. The key reaction led to the formation of cyclic imidates in good yield and with high regioselectivity. It was demonstrated that the cyclic imidates may be readily converted into 1,3-amino alcohols. Inco...

Abstract α-Pyridones and α-pyrones are ubiquitous structural motifs found in natural products biologically active small molecules. Here, we report an Rh-catalyzed electrochemical vinylic C–H annulation of acrylamides with alkynes, affording cyclic good to excellent yield. Divergent syntheses α-pyridones imidates accomplished by employing N- phenyl tosyl as substrates, respectively. Additionally...

A synthesis of functionalized fused pyrimidine derivatives from the respective ortho-nitroaromatic carboximes is described. Commercially available nitroarenes were transformed according to a known manner into the ortho-nitroaromatic carboximes. Selective catalytic reduction of the nitro group in these compounds followed by condensation of the amines formed with various orthoesters, resulted in ...

The cleavage and addition of ortho C-H bonds in various aromatic compounds such as ketones, esters, imines, imidates, nitrile, and aldehydes to olefins and acetlylenes can be achieved catalytically with the aid of ruthenium catalysts. The reaction is generally highly efficient and useful in synthetic methods. The coordination to the metal center by a heteroatom in directing groups such as carbo...

ABSTRACT. A series of nine new 6-aryl-7-alkyl/aryl-[1,2,4]triazolo[4,3-a][1,3,5]triazine-5(6H)-thiones (2a-i) were synthesized by a reaction N-triazol-3-yl imidates (1) with three different isothiocyanate derivatives (RNCS) in refluxing toluene. The structures the final heterocyclic compounds confirmed 1H-NMR, 13C-NMR, FT-IR, elemental analysis, and mass spectral analysis. target vitro screened...