The Total Synthesis of (±)-Hinesol and (±)-Agarospirol
The Total Synthesis of (±)-Hinesol and (±)-Agarospirol作者机构:Department of Fine Chemistry Jilin Chemical Engineering College Jilin 132002 China Department of Chemistry Qing Hua University Beijing 100084 China
出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))
年 卷 期:1997年第8卷第11期
页 面:957-960页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学]
主 题:The Total Synthesis of Hinesol and Agarospirol
摘 要:A mild base-catalyzed retro-benzilic acid rearrangement of a proto-[2+2]photocycloadduct, formed in highly steroselective photoaddition of methyl 2,4-dioxo-pentanoate to 1,5-dimethyl-6-methylenecyclohexene, afforded a spiro[4, 5] decenedione from which hinesol and agarospirol were synthesized by means of reductive elimination of α-diketone and C1-homologation.