SYNTHETIC STUDIES ON IRIDOID TERPENES VIA REGIOSELECTIVE SULFENYLATION OF β-KETOESTERS AND OXIDATIVE CLEAVAGE OF β-THIOALCOHOLS —A NOVEL SYNTHETIC ROUTE TO (±)-LOGANIN—
作者:Kunio Hiroi、Hideyuki Miura、Kumiko Kotsuji、Shuko Sato
DOI:10.1246/cl.1981.559
日期:1981.4.5
Regioselective sulfenylation of ethyl 2-oxocyclopentanecarboxylate (3) and methyl 7 , 7-ethylenedioxy-3-oxobicyclo [3.3.0] octane-2-carboxylate (12), followed by NaBH4 reduction and subsequent oxidative ring cleavage with lead(IV) acetate gave ethyl 2-acetoxy-6-phenylthio-2,3,5,6-tetrahydro-4H-pyran-3-carboxylate (7) and methyl 3-acetoxy-6,6-ethylenedioxy-1,3,4,4a,5,6,7,7a-octahydro-l-phenylthiocy
2-氧代环戊烷羧酸乙酯 (3) 和 7 , 7-亚乙基二氧基-3-氧代双环 [3.3.0] 辛烷-2-羧酸甲酯 (12) 的区域选择性亚磺酰化,然后是 NaBH4 还原,随后用乙酸铅 (IV) 进行氧化环裂解得到2-乙酰氧基-6-苯硫基-2,3,5,6-四氢-4H-吡喃-3-羧酸乙酯(7)和3-乙酰氧基-6,6-亚乙基二氧基-1,3,4,4a甲酯, 5,6,7,7a-八氢-1-苯基硫代环戊二烯[c]吡喃-4-羧酸酯(15)。硫代缩醛(7 和 15)的水解产生了环烯醚萜烯的特征 5,6-二氢-6-羟基-4H-吡喃-3-羧酸酯。