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 …

In this review we describe the various new methodologies for synthetic postmodification of
the BODIPY core designed and developed by our research groups, as well as their …

BODIPY dyes are well-known for their outstanding features, such as solubility in a wide
range of solvents, useful photophysical properties, and good photochemical and thermal …

Boron-dipyrromethene dyes (BODIPYs) containing halogens at pyrrole carbons are very
useful synthons for the synthesis of a variety of BOIDPYs for a wide range of applications …

A general and efficient method for α-chlorination of 4, 4′-difluoro-4-bora-3a, 4a-diaza-s-
indacenes (BODIPYs) has been developed using CuCl2 as chlorination reagent. The …

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 …

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

Cross-coupling reactions have played a key role in producing numerous types of π-
conjugated small molecules having appealing properties for practical applications in organic …

Simple organic molecules (SOM) based on bis (haloBODIPY) are shown to enable circularly
polarized luminescence (CPL), giving rise to a new structural design for technologically …

A one‐step synthetic procedure for the radical C H alkylation of BODIPY dyes has been
developed. This new reaction generates alkyl radicals through the oxidation of boronic acids …