作者:B.V. Subba Reddy、B. Phaneendra Reddy、N. Swapnil、J.S. Yadav
DOI:10.1016/j.tetlet.2013.08.043
日期:2013.10
A concise approach for the total synthesis of attenols A and B is described involving MacMillan’s α-aminooxylation, Evan’s asymmetric alkylation, Brown’s allylation, and spiro-ketalization as key steps. This approach has successfully demonstrated the α-aminooxylation protocol for the construction of the anti-1,3-diol unit.
描述了一种简单的全合成甜醇A和B的方法,其中涉及MacMillan的α-氨基氧基化,Evan的不对称烷基化,Brown的烯丙基化和螺缩酮化作为关键步骤。该方法已成功证明了用于构建抗-1,3-二醇单元的α-氨基氧基化方案。