Rhodium-Catalyzed Relay Carbenoid Functionalization of Aromatic C–H Bonds toward Fused Heteroarenes

Abstract

A rhodium-catalyzed annulation between ethyl benzimidates and α- aroyl sulfur ylides was developed, affording a series of pyrano­[4,3,2-<i>ij</i>]­isoquinoline derivatives in moderate to good yields with good functional group compatibility. The procedure featured dual <i>ortho</i>-C–H functionalization and dual cyclization in one pot. The optoelectronic properties of those fused heteroarenes were tested by UV/vis and fluorescence spectrometers

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