Kim Woo Han, Angeles Angie R, Lee Jun Hee, Danishefsky Samuel J
Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, NY 10065, USA.
Tetrahedron Lett. 2009 Nov 25;50(47):6440-6441. doi: 10.1016/j.tetlet.2009.08.131.
We describe herein a concise synthesis of an intermediate, via 2,3-Wittig rearrangement and Williamson etherification, en route to the natural products, xenibellols A and B.
我们在此描述了一种中间体的简洁合成方法,该方法通过2,3-维蒂希重排和威廉姆森醚化反应,用于合成天然产物西尼贝醇A和B。