Julia-Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactones
被引:46
作者:
Chen, WP
论文数: 0引用数: 0
h-index: 0
机构:
Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, EnglandUniv Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
Chen, WP
[1
]
Roberts, SM
论文数: 0引用数: 0
h-index: 0
机构:
Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, EnglandUniv Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
Roberts, SM
[1
]
机构:
[1] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1999年
/
02期
关键词:
D O I:
10.1039/a808436j
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The enone 1 was oxidized stereoselectively using urea-hydrogen peroxide with polyleucine as the catalyst to give the epoxide 2 which was used to make (+)-goniotriol 7, (+)-goniofufurone 8, (+)-8-acetylgoniotriol 9 and goniopypyrone 10.