Regiospecific β-lactam ring-opening/recyclization reactions of N-aryl-3-spirocyclic-β-lactams catalyzed by a Lewis–Brønsted acids combined superacid catalyst system: a new entry to 3-spirocyclicquinolin-4(1H)-ones-Reference-Cited by-同舟云学术

Regiospecific β-lactam ring-opening/recyclization reactions of N-aryl-3-spirocyclic-β-lactams catalyzed by a Lewis–Brønsted acids combined superacid catalyst system: a new entry to 3-spirocyclicquinolin-4(1H)-ones

Published:2012 Issue:5 Volume:48 Page:690-692
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Hu Yinqiao,Fu Xiaolan,Barry Badru-Deen,Bi Xihe,Dong Dewen

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/2012/CC/C1CC15881C

Reference22 articles.

1. For a general review on ‘β-Lactams’, see: Heterocyclic Scaffolds I: β-Lactams, in Top. Heterocycl Chem, ed. B. K. Banik, Springer-Verlag, Berlin Heidelberg, 1st edn, 2010, vol. 22

2. β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products

3. Efficient and Practical Method for Synthesizing N-Heterocyclic Compounds Using Intramolecular Nucleophilic Acyl Substitution Reactions Mediated by Ti(O-i-Pr)4/2i-PrMgX Reagent. Synthesis of Quinolones, Pyrroles, Indoles, and Optically Active N-Heterocycles Including Allopumiliotoxin Alkaloid 267A

4. An Intramolecular Rearrangement of 1-Arylazetidin-2-ones in an Acidic Solution

5. Formation of 2,3-dihydro-4(1H)-quinolones and related compounds via Fries-type acid-catalysed rearrangement of 1-arylazetidin-2-ones

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