期刊:Synlett [Thieme Medical Publishers (Germany)] 日期:2003-01-01卷期号: (14): 2185-2187被引量:26
标识
DOI:10.1055/s-2003-42071
摘要
The asymmetric total synthesis of attenol A (1) and B (2), which possess challenging structures and an interesting biological activity, was accomplished in a convergent and highly stereoselective manner (de, ee ≥ 96%) with good overall yield. The short total synthesis is based on asymmetric alkylations of SAMP-hydrazones as well as a Sharpless asymmetric dihydroxylation as key steps.