Fluorophores based on the 4-bora-3a, 4a-diaza-s-indacene (aka boron dipyrromethene,
boron dipyrrin, or BODIPY) platform have found diverse applications in different fields of …

BODIPYs (Boron-dipyrromethenes) are a class of fluorophores widely used in a plethora of
scientific applications in material science and biomedicine due to their exceptional optical …

Unsymmetrically substituted boron (III) and zinc (II) dipyrromethenates were synthesized in
high yields, and the physico-chemical investigation results of them are presented …

A copper-catalyzed direct C–H arylation or vinylation of BODIPYs at the β-position by
iodonium salts has been developed, which provides facile access to a variety of mono …

The results of investigation of the spectral characteristics, photostability and thermal
degradation of B (III) and Zn (II) complexes with 3, 3′, 5, 5′-tetramethyl-2, 2 …

The versatility in the synthesis of BODIPY derivatives in terms of functionalization is further
demonstrated. In particular, in this work β–β′-BODIPY dimers with varied functional groups …

A classical, safe and efficient red-shift strategy contributing to NIR arylacetylene-containing
rhodamines has been developed via the desulfitative Sonogashira cross-coupling reaction …

A series of complex boronic acids were prepared through multicomponent reactions
(MCRs). Both Passerini and Ugi MCRs were carried out in which one component was an …

Amino acid sensing is a powerful tool for intra-and extra-cellular assays. We report herein
the generation and optimization of bioconjugatable fluorescent reporter for pan-amino acid …