An approach to the synthesis of 5,5-trans-fused lactam analogues of β-lactam antibiotics-Reference-Cited by-同舟云学术

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An approach to the synthesis of 5,5-trans-fused lactam analogues of β-lactam antibiotics

Published:2001 Issue:1 Volume: Page:21-25
ISSN:1472-7781
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Smith Paul W.,Whittington Andrew R.,Cobley Kevin N.,Jaxa-Chamiec Albert,Finch Harry

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2001/P1/B007286I

Cited by 16 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. KOH-catalyzed regioselective ring openings of N-tosylaziridines with malonates in acetone;Journal of Molecular Catalysis A: Chemical;2012-11

2. Catalytic Asymmetric Ring-Opening ofmeso-Aziridines with Malonates under Heterodinuclear Rare Earth Metal Schiff Base Catalysis;Journal of the American Chemical Society;2011-04-20

3. Lewis Acid Catalyzed Highly Stereoselective Domino-Ring-Opening Cyclization of Activated Aziridines with Enolates: Synthesis of Functionalized Chiral γ-Lactams;The Journal of Organic Chemistry;2010-09-17

4. ChemInform Abstract: An Approach to the Synthesis of 5,5-trans-Fused Lactam Analogues of β-Lactam Antibiotics.;ChemInform;2010-05-26

5. Catalytic hydrogenation of methyl esters of some 1h-pyrazoline-3-carboxylic acids;Chemistry of Heterocyclic Compounds;2009-10

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