The azomethine ylide strategy for β-lactam synthesis: the structure of the key 1,3-dipolar intermediate-Reference-Cited by-同舟云学术

The azomethine ylide strategy for β-lactam synthesis: the structure of the key 1,3-dipolar intermediate

Published:1997 Issue:19 Volume: Page:1897
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

R. Martel Sarah,Planchenault Denis,Wisedale Richard,Gallagher Timothy,R. Martel Sarah,Planchenault Denis,J. Hales Neil

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/1997/CC/A704099G

Reference16 articles.

1. β-Lactam-Based Azomethine Ylide Reactivity. Expedient Synthesis of Carbapenams and Carbapenems

2. A Direct and Convergent Approach to Penams and Penems

3. XY–ZH systems as potential 1,3-dipoles. Part 11. Stereochemistry of 1,3-dipoles generated by the decarboxylative route to azomethine ylides

4. XY–ZH systems as potential 1,3-dipoles. Part 12. Mechanism of formation of azomethine ylides via the decarboxylative route from α-amino acids

5. Evidence for an azomethine ylide intermediate in the carbonyl- assisted decarboxylation of sarcosine. Novel synthesis of dl-phenylephrine hydrochloride

Cited by 12 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. Metal-free Decarboxylative Amination: An Alternative Approach Towards Regioselective Synthesis of β-CarbolineN-fused Imidazoles;Advanced Synthesis & Catalysis;2017-01-27

2. Synthesis and Reactivity of 2-(Carboxymethyl)aziridine Derivatives;Chemical Reviews;2014-04-28

3. ChemInform Abstract: The Azomethine Ylide Strategy for β-Lactam Synthesis: The Structure of the Key 1,3-Dipolar Intermediate.;ChemInform;2010-06-24

4. Azetidines, Azetines and Azetes: Monocyclic;Comprehensive Heterocyclic Chemistry III;2008

5. S-Alkyl Dithioformates as 1,3-Dipolarophiles. Generation of C(2)-Unsubstituted Penems;Organic Letters;2004-07-02