An efficient total synthesis of (−)-mintlactone and (+)-isomintlactone
摘要:
Total synthesis of (-)-mintlactone and (+)-isomintlactone has been achieved diastereoselectively via a fused butenolide construction strategy based on an intramolecular [3+2] cycloaddition reaction of nitrile oxide.
An efficient total synthesis of (−)-mintlactone and (+)-isomintlactone
摘要:
Total synthesis of (-)-mintlactone and (+)-isomintlactone has been achieved diastereoselectively via a fused butenolide construction strategy based on an intramolecular [3+2] cycloaddition reaction of nitrile oxide.
[EN] PREPARATION OF 3-HYDROXY-3,6-DIMETHYLHEXAHYDROBENZOFURAN-2-ONE AND DERIVATIVES THEREOF<br/>[FR] PRÉPARATION DE 3-HYDROXY-3,6-DIMÉTHYLHEXAHYDROBENZOFURAN-2-ONE ET DE DÉRIVÉS DE CELLE-CI
申请人:P2 SCIENCE INC
公开号:WO2017044957A1
公开(公告)日:2017-03-16
The present invention relates to the synthesis of intermediate compounds which can be used in the synthesis of mint lactone and related compounds, including 3,6-dimethylhexahydrobenzofuran-2-ones, isomers, and other derivatives.
An efficient total synthesis of (−)-mintlactone and (+)-isomintlactone
作者:Kozo Shishido、Osamu Irie、Masayuki Shibuya
DOI:10.1016/s0040-4039(00)61320-5
日期:1992.8
Total synthesis of (-)-mintlactone and (+)-isomintlactone has been achieved diastereoselectively via a fused butenolide construction strategy based on an intramolecular [3+2] cycloaddition reaction of nitrile oxide.