Shepherd Jennifer N, Myles David C
Department of Chemistry, Gonzaga University, Spokane, Washington 99258, USA.
Org Lett. 2003 Apr 3;5(7):1027-30. doi: 10.1021/ol027538p.
[reaction: see text] Diastereoselective acetalization of pseudo-C(2)-symmetric 1,3,5-triol systems is a general strategy for the rapid generation of polyketides. The oxidative acetalization reaction shown above was studied under both kinetic and thermodynamic conditions, using synthetic 1,3,5-triol units. In addition, all possible stereochemical variants of a 1,3,5-triol system were prepared from the corresponding acetal to expand the synthetic versatility of this method.
[反应:见正文] 假C(2)-对称1,3,5-三醇体系的非对映选择性缩醛化是快速生成聚酮化合物的通用策略。使用合成的1,3,5-三醇单元,在动力学和热力学条件下研究了上述氧化缩醛化反应。此外,由相应的缩醛制备了1,3,5-三醇体系的所有可能的立体化学变体,以扩展该方法的合成通用性。