A NEW ENANTIOSELECTIVE SYNTHESIS OF THE AMINODIHYDROISOCOUMARIN MOIETY OF AI-77-B

被引:23
作者
KOTSUKI, H
MIYAZAKI, A
OCHI, M
机构
关键词
D O I
10.1246/cl.1992.1255
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aminodihydroisocoumarin moiety of AI-77-B, a gastroprotective substance isolated from Bacillus pumilus AI-77, has been prepared from a convenient chiral synthon of L-erythrose by combination of chiral triflate technology and regioselective aromatic carboxylation.
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页码:1255 / 1258
页数:4
相关论文
共 5 条
[1]  
Gschwend H.W., 1979, ORG REACT, V26, P1
[2]   SUPERBASES FOR ORGANIC-SYNTHESIS [J].
SCHLOSSER, M .
PURE AND APPLIED CHEMISTRY, 1988, 60 (11) :1627-1634
[3]   ACTIVATION OF ORGANOLITHIUM REAGENTS [J].
SCHLOSSER, M .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1967, 8 (01) :9-+
[4]   DIRECTED ORTHO METALATION - TERTIARY AMIDE AND O-CARBAMATE DIRECTORS IN SYNTHETIC STRATEGIES FOR POLYSUBSTITUTED AROMATICS [J].
SNIECKUS, V .
CHEMICAL REVIEWS, 1990, 90 (06) :879-933
[5]   REGIOSELECTIVE SYNTHETIC PROCESSES BASED ON THE AROMATIC DIRECTED METALATION STRATEGY [J].
SNIECKUS, V .
PURE AND APPLIED CHEMISTRY, 1990, 62 (04) :671-680