An Efficient and Stereoselective Synthesis of the 1β-Methylcarbapenem Key Precursor
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/4/19_4_531/_pdf
Reference7 articles.
1. Synthetic Carbapenem Antibiotics. I. 1-b-Methylcarbapenem
2. Synthesis of the 1.BETA.-methylcarbapenem key intermediates.
3. Synthetic Studies on Carbapenem Antibiotics: A Carbon-introduced Reaction at the C-4 Position of a b-Lactam by Carbane Insertion Reaction
4. A Novel Carbon-Carbon Bond Forming Reaction by Means of Sulfur-Ylide Rearrangement and Its Application to the Synthesis of Physiologically Active Compounds
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Preparations of two pivotal intermediates for the synthesis of 1-β-methyl carbapenem antibiotics;Tetrahedron;1996-01
2. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996
3. Other Fused Azetidines, Azetines, and Azetes;Comprehensive Heterocyclic Chemistry II;1996
4. Synthesis of the 1β-Methylcarbapenem Key Intermediates;Stereoselective Synthesis;1993
5. Chemistry of O-silylated ketene acetals: an efficient synthesis of carbapenem and 1β-methylcarbapenem intermediates;J. Chem. Soc., Perkin Trans. 1;1992
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