Enantioselective synthesis of epoxides and aziridines by asymmetric methylidene transfer from a sulfimide to carbonyl compounds and imines
被引:22
作者:
Baird, CP
论文数: 0引用数: 0
h-index: 0
机构:
Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, EnglandUniv Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
Baird, CP
[1
]
Taylor, PC
论文数: 0引用数: 0
h-index: 0
机构:
Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, EnglandUniv Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
Taylor, PC
[1
]
机构:
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1998年
/
20期
关键词:
D O I:
10.1039/a805405c
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The sodium salt of sulfimide 2 is a useful asymmetric methylidene transfer agent for the synthesis of enantiomerically enriched epoxides and aziridines. Moderate enantioselectivities are observed with a broad range of carbonyl compounds and with imines. An enantiomerically enriched beta-adrenoreceptor agonist analogue was prepared using the new method.