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β-Carboline directed regioselective hydroxylation by employing Cu(OAc)2 and mechanistic investigation by ESI-MS†
Darshana Bora,Ramya Tokala,Stephy Elza John,Bitla Prasanth,Nagula Shankaraiah
Organic & Biomolecular Chemistry Pub Date : 03/04/2020 00:00:00 , DOI:10.1039/D0OB00250J
Abstract

A β-carboline directed regioselective C–H activation protocol for hydroxylation has been developed by employing Cu(OAc)2, a cost-effective 3d metal. This fastidious reaction proceeds under microwave irradiation and furnishes exclusively ortho-hydroxylated products with moderate to good yields under greener reaction conditions. Gratifyingly, this approach retains considerable functional group tolerance and is feasible on both electron-rich and electron-deficient substrates. This protocol signifies monohydroxylation on β-carboline via C–H functionalization which leads into development of biologically relevant molecules. The reaction mechanism was confirmed by intercepting and characterizing all the proposed intermediates by ESI-QTOF-MS.

Graphical abstract: β-Carboline directed regioselective hydroxylation by employing Cu(OAc)2 and mechanistic investigation by ESI-MS
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