1.
Org Lett
; 26(23): 4857-4862, 2024 Jun 14.
Artículo
en Inglés
| MEDLINE
| ID: mdl-38838191
RESUMEN
The efficient construction of π-conjugated polycyclic heteroarenes represents a significant task in the field of functional materials. A one-step oxidative tandem cyclization of aromatic acids with (benzo)thiophenes was developed to access planar sulfur-containing polycyclic heteroarenes. This protocol undergoes intermolecular cross-dehydrogenative coupling followed by intramolecular Friedel-Crafts acylation and provides a facile pathway to planar polycyclic compounds from inexpensive reactants. The synthesized heteroarenes serving as lipid-droplet-targeted probes exhibit outstanding performance with favorable biocompatibility and photostability.
2.
Chin Med J (Engl)
; 133(20): 2515-2517, 2020 Oct 20.
Artículo
en Inglés
| MEDLINE
| ID: mdl-32941238
3.
Chin Med J (Engl)
; 133(2): 235-236, 2020 Jan 20.
Artículo
en Inglés
| MEDLINE
| ID: mdl-31868802