Photoactivatable (alternatively, photoremovable, photoreleasable, or photocleavable)
protecting groups (PPGs), also known as caged or photocaged compounds, are used to …

Julolidines constitute a class of N‐heterocycle compounds which have in common the 2, 3,
6, 7‐tetrahydro‐1H, 5H‐benzo [1, 2] quinolizine ring. Due mainly to its fluorescence …

A new class of coumarin photocaging groups modified with an electron‐rich styryl moiety at
the 3‐position was constructed. The large π‐conjugated structure and stabilization of the …

1, 5-hydride transfer-triggered cyclization reactions offering a robust method for C (sp3)–C
(sp3) coupling and the synthesis of eg tetrahydroquinolines have been thoroughly …

The possibilities of dicyanocoumarin (DCCM)‐modified oligonucleotides are expanded to
not just allow their release and therefore activation with green light (OFF→ ON) but to also …

The development of light‐responsive molecular tools enables spatiotemporal control of
biochemical processes with superior precision. Amongst these molecular tools, photolabile …

New coumarin fused oxazoles were investigated as photosensitive units for carboxylic acid
groups using butyric acid as a model compound. 6-Oxo-6H-benzopyrano [6, 7-d] oxazol-8 …

Abstract Ala–Ala–Pro–Val (AAPV) is a bioactive tetrapeptide that inhibits human neutrophil
elastase, an enzyme involved in skin chronic inflammatory diseases like psoriasis. Caged …

Aim ng at the improvement of the photorelease of butyric acid–a model carboxylic acid drug,
a set of heteroaromatic compounds based on acridine, naphtho [2, 1-b] pyran, 3H …

The Pechmann condensation of phenolic fluorenes with ethyl acetoacetate afforded indene-
fused 4-methylcoumarins. In addition to the expected indeno [1, 2-g] coumarin, a skeletal …