Exploring the Border between Concerted and Two-Step Pathways of 1,3-Dipolar Cycloadditions of Organic Azides to Cyclic Ketene N,X-Acetals. - Synthesis and15N-NMR Spectra of Zwitterions and Spirocyclic Cycloadducts-Reference-Cited by-同舟云学术

Exploring the Border between Concerted and Two-Step Pathways of 1,3-Dipolar Cycloadditions of Organic Azides to Cyclic Ketene N,X-Acetals. - Synthesis and15N-NMR Spectra of Zwitterions and Spirocyclic Cycloadducts

Published:2005-06 Issue:6 Volume:88 Page:1589-1609
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Quast Helmut,Ach Manfred,Balthasar Jürgen,Hergenröther Thomas,Regnat Dieter,Lehmann Jens,Banert Klaus

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference67 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. Kinetics and Mechanism of 1,3-Dipolr Cycloadditions

3. in ‘The Chemistry of Alkenes’, Ed. S. Patai, 1st edn., John Wiley & Sons, New York, 1964, Chapt. 11, p. 835-844;

4. in ‘1,3-Dipolar Cycloaddition Chemistry’, Ed. A. Padwa, 1st edn., John Wiley & Sons, New York, 1984, Vol. 1, Chapt. 1;

5. in ‘Advances in Cycloaddition’, Ed. D. P. Curran, 1st edn., JAI Press, London, 1988, Chapt. 1.

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