Ortho-Alkynylbenzaldehydes have been widely used to generate isochromenylium derivatives through gold-catalyzed cycloisomerization. These isochromenylium derivatives have been exploited as formal diene derivatives for reactions with different dienophiles. Herein, we describe the behavior of ortho-alkynylsalicylaldehydes, a particular case of ortho-alkynylbenzaldehydes. The gold-catalyzed cycloisomerization of ortho-alkynylsalicylaldehydes delivers an unusual heterodiene derivative that reacts with electron-rich alkenes through a formal [4+2] cycloaddition. In this reaction, both the diene and dienophile are generated in situ through gold-catalyzed cycloisomerization of appropriate alkynamines or alkynols. This reaction was used to synthesize complex tetracyclic pyrano[2,3,4-de]chromenes from two very simple starting materials (an ortho-alkynylsalicylaldehyde and an alkynamine or alkynol) with complete atom economy and with selective formation of bonds, cycles, and stereocenters.
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Arto et al. (2016) studied this question.
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