CHIRAL SYNTHESIS OF THE KEY INTERMEDIATE FOR 1-BETA-METHYLCARBAPENEM ANTIBIOTICS STARTING FROM (-)-CARVONE
被引:8
作者:
HONDA, T
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机构:
HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPANHORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
HONDA, T
[1
]
ISHIZONE, H
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HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPANHORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
ISHIZONE, H
[1
]
MORI, W
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HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPANHORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
MORI, W
[1
]
NAITO, K
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HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPANHORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
NAITO, K
[1
]
SUZUKI, Y
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HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPANHORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
SUZUKI, Y
[1
]
机构:
[1] HORIUCHI ITARO CO LTD,HIGASHIMURAYAMA,TOKYO 189,JAPAN
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1991年
/
12期
关键词:
D O I:
10.1039/p19910003027
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A stereoselective synthesis of the key intermediate for the preparation of 1-beta-methylcarbapenem antibiotics was achieved by using a cyclopentanone derivative, easily derived from (-)-carvone, as a starting material.