期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 124, 期 12, 页码 2951-2956出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja0174027
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资金
- NCI NIH HHS [CA 85419] Funding Source: Medline
The first total synthesis of the potent antitumor antibiotic (-)-tetrazomine has been accomplished. A new method for the formation of the allylic amine precursor to an azomethine ylide has been developed and exploited in an efficient [1,3]-dipolar cycloaddition to afford the key tetracyclic intermediate used in the synthesis of (-)-tetrazomine. Several analogues of tetrazomine have been synthesized and tested for antimicrobial and biochemical activity.
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