Litcius/Paper detail

Cobalt(II)porphyrin-Mediated Selective Synthesis of 1,5-Diketones via an Interrupted-Borrowing Hydrogen Strategy Using Methanol as a C1 Source

Priyabrata Biswal, Shaikh Samser, Prakash Nayak, Vadapalli Chandrasekhar, Krishnan Venkatasubbaiah

2021The Journal of Organic Chemistry24 citationsDOI

Abstract

A novel cobalt(II)porphyrin-mediated acceptorless dehydrogenation of methanol is reported for the first time. This methodology has been applied for the coupling of a variety of ketones with methanol to produce 1,5-diketones along with H2 and H2O as the environment friendly byproducts. This paradigm was also demonstrated for a one-pot synthesis of substituted pyridines using a sequential addition protocol where the 1,5-diketones were generated in situ. From many experiments including those involving deuterium labeling, it is proposed that protonated cobalt(II)porphyrin methoxide complex acts as an intermediate to generate formaldehyde along with a metal hydride.

Topics & Concepts

ChemistryCobaltPorphyrinMethanolHydrideDehydrogenationProtonationMethoxideCombinatorial chemistryFormaldehydePhotochemistryMetalCatalysisOrganic chemistryIonAsymmetric Hydrogenation and CatalysisFluorine in Organic ChemistryChemical Synthesis and Analysis