A total synthesis of (−)-reiswigin a via sequential claisen rearrangement-intramolecular ester enolate alkylation
作者:Deukjoon Kim、Kye Jung Shin、Ik Yoen Kim、Sang Woo Park
DOI:10.1016/0040-4039(94)80021-9
日期:1994.10
(−)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesized in a highly stereoselective manner utilizing a sequential Claisen rearrangement — intramolecular ester enolate alkylation strategy.
(-)-Reiswigin A(1),一种新型的抗病毒二萜,已经通过使用顺序Claisen重排-分子内酯烯醇化烷基化策略以高度立体选择性的方式合成。