- 作者: 王進欣、李瀛、張朝欣
- 作者服務機構: National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, 730000, P. R. China
- 中文摘要: The optically active β-hydroxyl-γ-butyrolactones were synthesized from nonchiral starting material by employing reductive cleavage reaction, sharpless asymmetric epoxidation and dihydroxylation, and Lewis acid-catalysed cyclization as key steps. This strategy can be used to prepare many chiral β-hydroxyl-γ-butyrolactone analogues.
- 英文摘要: --
- 中文關鍵字: Asymmetric synthesis; β-Hydroxy-γ-butyrolactone; Reductive cleavage reaction; Sharpless epoxidation and dihydroxylation; Cyclization.
- 英文關鍵字: --