The use of boron dipyrromethene (BODIPY) in biomedicine is reviewed. To open, its
synthesis and regulatory strategies are summarized, and inspiring cutting‐edge work in post …

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 …

Bacterichlorins possess a characteristic intense electronic absorption in the near-infrared
part of the electromagnetic radiation (NIR) from 700 nm up to 900 nm, where endogenous …

The BODIPYs are a very widely used class of fluorescent dyes, based around a heterocyclic
organic framework, which have found applications across a broad range of research areas …

Boron-dipyrromethene (BODIPY) dyes have been extensively investigated in recent years
for a variety of bioanalytical and bioimaging applications. The success of these applications …

Regioselective and stepwise syntheses of a series of functionalized BODIPY dyes through
palladium-catalyzed cross-coupling reactions and direct C–H arylations have been …

Regioselective functionalization of 2, 3, 5, 6, 8-pentachloro-BODIPY 1 produced
unsymmetric BODIPY 5, bearing an isothiocyanate group suitable for conjugation, in only …

A series of push–pull BODIPYs bearing multiple electron-donating and electron-acceptor
groups were synthesized regioselectively from 2, 3, 5, 6, 8-pentachloro-BODIPY, and …

The presence of F or CN substituents at boron in BODIPYs causes a dramatic effect on their
reactivity, which allows their chemoselective postfunctionalization. Thus, whereas 1, 3, 5, 7 …

Oxidative nucleophilic α-hydrogen substitution is a direct method for BODIPY
functionalization. However, it was hampered by the low reactivity of BODIPYs toward weak …