Organic Chemistry Division-I, CSIR-Indian Institute of Chemical Technology, Hyderabad 500 007, India.
J Org Chem. 2011 Dec 2;76(23):9835-40. doi: 10.1021/jo201570h. Epub 2011 Nov 1.
Efficient total syntheses of (+)-pyrenolide D (5) and (-)-4-epi-pyrenolide D (6) have been achieved from a known 5-deoxy-d-xylose derivative 9 in ten steps with 19% overall yield either exclusively as 5 or as pure 5 and 6 in a 3:2 ratio. Key steps involved are one-pot epoxidation-cyclization by Corey-Chaykvosky reagent, reductive Barton-McCombie deoxygenation, and per-acid mediated oxidative spiroketalization.
(+)-焦烯内酯 D(5)和(-)-4-表焦烯内酯 D(6)的高效全合成已从已知的 5-脱氧-D-木糖衍生物 9 经 10 步反应以 19%的总收率完成,其立体选择性地以 5 或纯 5 和 6(3:2 比例)形式获得。关键步骤包括 Corey-Chaykvosky 试剂一锅法环氧化-环化、还原 Barton-McCombie 脱氧和过酸介导的氧化螺缩酮化。