Tunable Phosphine‐Mediated Domino Reaction: Selective Synthesis of 2,3‐Dihydrofurans and Biaryls

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We have developed a novel strategy to control the product distribution between 2,3‐dihydrofurans and biaryls from the same starting materials by tuning the catalytic or stoichiometric process. By controlling the loading of the phosphine PR3, the Morita–Baylis–Hillman carbonates can be selectively used as a C1 or a C3 synthon, respectively. This investigation has given new insights into tunable domino reactions and will be useful in diversity‐oriented synthesis (DOS).

Document Type: Research Article

DOI: http://dx.doi.org/10.1002/adsc.201200675

Affiliations: State Key Laboratory and Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, People's Republic of China, Fax: (+86)-22-2350-3627

Publication date: January 14, 2013

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