In the presence of triphenylphosphine, copper (II) chloride can catalyze an intermolecular
ortho-acylation reaction of phenols with aryl aldehydes. The reaction proceeds smoothly …

Xanthones belong to a class of O-heterocycles which are known for their great variety of
biological/pharmacological activities. The xanthone scaffold can be considered as a …

H‐bonding, as a non covalent stabilizing interaction of diverse nature, has a central role in
the structure, function and dynamics of chemical and biological processes, pivotal to …

This review demonstrates that oximes and their derivatives are valuable starting materials
for the preparation of many classes of heterocyclic compounds. The main group of reactions …

A versatile and highly efficient strategy to construct a xanthone skeleton via a ligand-free
intermolecular catalytic coupling of 2-substituted benzaldehydes and a wide range of …

We report an efficient, selective, rapid and eco-friendly protocol for the one-step synthesis of
a small xanthone library via an intermolecular catalytic coupling from readily available …

A series of 2, 2′‐dihydroxybenzophenones and their carbonyl N‐analogues were studied
as potential inhibitors against human glutathione transferase M1‐1 (hGSTM 1‐1) purified …

Naphtho [1, 8-de][1, 2] oxazin-4-ol and its acyl or benzyl derivatives ring open to various 2, 8-
dihydroxy-1-naphthonitriles, which, through (de) protection protocols and reduction, afford …

The MDR-involved human GSTA1-1, an important isoenzyme overexpressed in several
tumors leading to chemotherapeutic-resistant tumour cells, has been targeted by 2, 2 …

The selectivity of certain benzophenones and their carbonyl N‐analogues was investigated
towards the human GSTP 1‐1 allozymes A, B and C involved in MDR. The allozymes were …