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Palabras clave – provistas por la editorial

cross coupling; dearomatization; C-H functionalization; indolin-3-ones; dimerization and trimerization of indoles; C–H borylation; Sonogashira cross-coupling; borylated aryl alkynes; one-pot reaction; restricted rotations; M(CO)3 tripods; molecular brakes and gears; X-ray; V-T NMR; borylation; Suzuki coupling; NH-Free; 5-aryl pyrrole-2-carboxylates; iridium-catalyzed; heteroaryl substituted pyrroles; 2,3′-bipyrrole; electrophilic haloacetylenes; pyrroles; ethynylpyrroles; furans; thiophenes; pyrazoles; Al2O3; transition-metal catalysis; intramolecular cyclization; medium-sized heterocycles; C-H activation; acylation; palladium; arenes; heteroarenes; indigo dyes; DSSC; synthesis; spectroscopy; Heck reaction; styrene; methoxycarbonylation; profene; cross-coupling reactions; C-C bond forming reactions; C-Heteroatom bond forming reactions; clinical candidate; DNA-encoded libraries; cyclopeptides; allosteric modulators; PROTAC; catalysis in water; C–C cross-coupling; Suzuki–Miyaura reaction; sulfonated salan; n/a