Boron neutron capture therapy (BNCT) is a non‐invasive cancer treatment with little adverse
effect utilizing nuclear fission of 10B upon neutron irradiation. While neutron source has …

Boron subphthalocyanines bearing a wide range of functional groups were tested as
prospective photosensitizers and fluorophores. Synthetic protocols to novel 4 …

Copper-containing agents are promising antitumor pharmaceuticals due to the ability of the
metal ion to react with biomolecules. In the current study, we demonstrate that inorganic …

Neutral and water soluble anionic carborane derivatives of 4, 4-difluoro-4-bora-3a, 4a-diaza-
s-indacene (BODIPY) were efficiently synthesized via nucleophilic aromatic substitution of p …

An efficient approach for the preparation of 3, 5-dicarborane-substituted BODIPY conjugates
was developed via the functionalization of 3, 5-dibromo-8-pentafluorophenyl-BODIPY with …

Two o-carborane-hybridized macrocyclic arenes have been synthesized via Friedel–Crafts
alkylation of carborane diaryl derivatives. The single-crystal X-ray diffraction analysis clearly …

Copper–organic compounds have gained momentum as potent antitumor drug candidates
largely due to their ability to generate an oxidative burst upon the transition of Cu2+ to Cu1+ …

2, 4, 6-Trichloro-1, 3, 5-triazine (cyanuric chloride) is an excellent coupling reagent for the
preparation of highly structured multifunctional molecules. Three component systems based …

A series of novel hybride ferrocene carborane derivatives containing allyl functionalities at
the carborane carbon atoms were firstly synthesized in a good yield providing their potential …

Carborane maleimides were prepared in good yields through the thermal cyclization of
maleamic acids prepared by the reaction of 3-amino-o-carborane with maleic or 3 …