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Use of aldolases in the synthesis of non-carbohydrate natural products. Stereoselective synthesis of aspicilin C-3—C-9 fragment

 

作者: Robert Chênevert,   Michèle Lavoie,   Mohammed Dasser,  

 

期刊: Canadian Journal of Chemistry  （NRC Available online 1997）
卷期: Volume 75, issue 1  

页码: 68-73

 

ISSN:0008-4042

 

年代: 1997

 

DOI:10.1139/v97-010

 

出版商: NRC Research Press

 

数据来源: NRC

 

摘要:

The C-3—C-9 main fragment of aspicilin was prepared via a fructose 1,6-diphosphate aldolase reaction. The same fragment was also synthesized by chemical transformation starting fromD-arabinose.Key words: aldolase, aspicilin, arabinose, synthesis.

 

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