Department of Organic Chemistry, Faculty of Pharmacy, University of Granada, 18071, Granada, Spain.
J Chem Ecol. 1991 Aug;17(8):1529-41. doi: 10.1007/BF00984686.
The synthesis of the title compound13 has been carried out through the preparation of its precursor, (3R,4R,5S,6R)-3,4,5-trihydroxy-1,7-dioxaspiro[5.5]undecane (6), obtained fromD-fructose using Wittig's methodology, reduction, and spiroketalation. Compound6 was transformed into13 by a Barton deoxygenation at C-5 followed by a Corey dideoxygenation at C-3,4 of the appropriately protected derivatives.
标题化合物 13 的合成是通过制备其前体(3R,4R,5S,6R)-3,4,5-三羟基-1,7-二氧杂螺[5.5]十一烷(6)来完成的,该前体是由 D-果糖通过Wittig 法、还原和螺缩酮化得到的。通过 Barton 在 C-5 脱氧和 Corey 在适当保护的衍生物的 C-3,4 去二氧,将化合物 6 转化为 13。