University of Berne, Department of Chemistry and Biochemsitry, Freiestrasse 3, CH-3012 Berne, Switzerland.
J Am Chem Soc. 2009 Dec 16;131(49):17746-7. doi: 10.1021/ja908933s.
A powerful intramolecular Schmidt reaction starting from primary azidoalcohols is reported. This approach involves a nonacidic activation of the alcohol via triflation. The synthetic potential offered by the mild reaction conditions is demonstrated by a highly selective synthesis of (-)-indolizidine 167B.
本文报道了一种从伯叠氮醇出发的强分子内施密特反应。该方法通过三氟甲磺酸酯活化醇,无需酸性条件。温和的反应条件提供了很大的合成潜力,通过该条件可以高立体选择性地合成(-)-indolizidine 167B。