A Novel Method for the Alkoxylation of Azetidin-2-ones at the 4-Position.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/40/4/40_4_1044/_pdf
Cited by 9 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. β-Lactam Ring Opening in the Reformatsky Reaction of (3R,4R)-4-Acetoxy-3-((1R)-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)azetidin-2-one with Ethyl 4-Bromo-3-oxopentanoate;Russian Journal of Organic Chemistry;2021-09
2. ChemInform Abstract: A Novel Method for the Alkoxylation of Azetidin-2-ones at the 4- Position.;ChemInform;2010-09-01
3. Diastereoselective construction of azetidin-2-ones by electrochemical intramolecular C–C bond forming reaction;Tetrahedron;2009-11
4. Tri-n-butyl(methoxy)stannane;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
5. P;Dictionary of Organic Compounds;1997
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