The State Key Laboratory of Elemento-Organic Chemistry and Department of Chemistry, Nankai University, 94 Weijin Road, Tianjin 300071, P.R. China.
Org Lett. 2011 Feb 18;13(4):580-3. doi: 10.1021/ol102738b. Epub 2011 Jan 14.
The phosphine-catalyzed annulations between Morita-Baylis-Hillman adduct carbonates and enones are reported. Under the catalysis of PBu(3) (20 mol %), cascade [3 + 2] cyclization-allylic alkylation, [2 + 2 + 1] annulation, and [3 + 2] cyclization reactions chemoselectively occur depending on the substituent variation of both the carbonate and enone. These reactions provide efficient syntheses of highly functionalized cyclopentenes and cyclopentanes.
报道了膦催化的 Morita-Baylis-Hillman 加合物碳酸酯与烯酮的环化反应。在 PBu(3) (20 mol %)的催化下,根据碳酸酯和烯酮取代基的变化,[3 + 2]环化-烯丙基烷基化、[2 + 2 + 1]环化和[3 + 2]环化反应可选择性地发生,从而实现了高度官能化的环戊烯和环戊烷的高效合成。