Aldehydes as Photoremovable Directing Groups: Synthesis of Pyrazoles by a Photocatalyzed [3+2] Cycloaddition/Norrish Type Fragmentation Sequence
Ana Pascual‐Escudero, Laura Ortiz‐Rojano, Silvia Simón‐Fuente, Javier Adrio, M. Ribagorda
Abstract
A straightforward methodology for the regioselective synthesis of pyrazoles has been developed by a domino sequence based on a photoclick cycloaddition followed by a photocatalyzed oxidative deformylation reaction. Distinguishing features of this protocol include an unprecedented photoredox-catalyzed Norrish type fragmentation under green-light irradiation and the use of α,β-unsaturated aldehydes as synthetic equivalents of alkynes, where the aldehyde is acting as a novel photoremovable directing group.
Topics & Concepts
ChemistryCycloadditionRegioselectivityAldehydeFragmentation (computing)DominoSequence (biology)Functional groupCombinatorial chemistryPhotochemistryOrganic chemistryCatalysisComputer sciencePolymerBiochemistryOperating systemRadical Photochemical ReactionsCatalytic C–H Functionalization MethodsOxidative Organic Chemistry Reactions