The effect of the change of synthetic route on the product 3393-45-1

This literature about this compound(3393-45-1)Reference of 5,6-Dihydro-2H-pyran-2-onehas given us a lot of inspiration, and I hope that the research on this compound(5,6-Dihydro-2H-pyran-2-one) can be further advanced. Maybe we can get more compounds in a similar way.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Regioselective Radical Borylation of α,β-Unsaturated Esters and Related Compounds by Visible Light Irradiation with an Organic Photocatalyst, published in 2021-06-04, which mentions a compound: 3393-45-1, Name is 5,6-Dihydro-2H-pyran-2-one, Molecular C5H6O2, Reference of 5,6-Dihydro-2H-pyran-2-one.

Radical hydroboration reactions have only recently been reported and are still rare. Here the authors describe a photoredox radical hydroboration of α,β-unsaturated esters, amides, ketones, and nitriles with NHC-boranes that uses only an organocatalyst and visible light. The conditions are mild, the substrate scope is broad, and the α/β regioselectivity is high. The reaction requires only the organocatalyst; there is no costly metal, and there are no other additives (base, cocatalyst, initiator).

This literature about this compound(3393-45-1)Reference of 5,6-Dihydro-2H-pyran-2-onehas given us a lot of inspiration, and I hope that the research on this compound(5,6-Dihydro-2H-pyran-2-one) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI