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Efficient Access to Orthoquinols and Their [4 + 2] Cyclodimers via SIBX-Mediated Hydroxylative Phenol Dearomatization

2007; American Chemical Society; Volume: 72; Issue: 16 Linguagem: Inglês

10.1021/jo0708893

1520-6904

Nathalie Lebrasseur, Julien Gagnepain, Aurélie Ozanne‐Beaudenon, Jean‐Michel Léger, Stéphane Quideau,

Catalytic C–H Functionalization Methods

SIBX, the nonexplosive formulation of the λ5-iodane 2-iodoxybenzioc acid (IBX), safely and efficiently mediates the hydroxylative dearomatization of various 2-alkylphenols and napthols into orthoquinols or their [4 + 2] cyclodimers. Reactions are typically run at room temperature using SIBX as a suspension in THF. Using these conditions, natural products such as the cyclodimer of the terpene carvacrol and, for the first time, the shikimate-derived (±)-grandifloracin were prepared in one step from their respective phenolic precursor.