Excited (triplet) states offer a myriad of attractive synthetic pathways, including
cycloadditions, selective homolytic bond cleavages and strain-release chemistry …

Triplet-triplet energy transfer (EnT) is a powerful activation pathway in photocatalysis that
unlocks new organic transformations and improves the sustainability of organic synthesis …

Radical remote 1, n-difunctionalization reactions (n> 2) of alkenes are powerful tools to
efficiently introduce functional groups with selected distances into target molecules. Among …

A new class of iminosulfonylation reagents were developed and extensively used in the 1, 2-
iminosulfonylation of various olefins. Olefins containing bioactive molecules, such as …

In the long-standing quest to synthesize fundamental building blocks with key functional
group motifs, photochemistry in the recent past has comprehensively established its …

Two C (sp3) radicals cross-coupling as a straightforward method for constructing C (sp3)–C
(sp3) bonds has attracted extensive attention from chemists. Unfortunately, the strategy is …

A general and environmentally friendly organic photo-induced strategy was developed for
the synthesis of diverse alkyl-substituted β-amino sulfone derivatives, including primary …

In this study, a metal-free difunctionalization strategy for diazenes was developed using a
range of bifunctionalization reagents. This strategy involves a unique N (sp3)–N (sp2) …

The 1, 2-iminylalkylation of diazenes using alkyl iodides in combination with an O-benzoyl
oxime is reported. In this transformation, O-benzoyl oxime acted as a radical precursor and …

We developed a highly selective and efficient multicomponent transformation by utilizing
alkynes and olefins/(hetero) arenes through photoinduced energy-transfer catalysis. The …