1,3-Dipolar Cycloadditions of Electrophilically Activated Benzonitrile N-Oxides. Polar Cycloaddition versus Oxime Formation-Reference-Cited by-同舟云学术

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1,3-Dipolar Cycloadditions of Electrophilically Activated Benzonitrile N-Oxides. Polar Cycloaddition versus Oxime Formation

Published:2006-11-15 Issue:25 Volume:71 Page:9319-9330
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Domingo Luis R.¹,Picher M. Teresa¹,Arroyo Pau¹,Sáez José A.¹

Affiliation:

1. Departamento de Química Orgánica, Universidad de Valencia, Dr. Moliner 50, 46100 Burjassot, Valencia, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0613986

Reference52 articles.

1. Wasserman, A.Diels−Alder Reactions; Elsevier: New York, 1965.

2. Padwa, A.1,3-Dipolar Cycloaddition Chemistry; Wiley-Interscience: New York, 1984; Vols. 1−2.

3. Huisgen, R.1,3-Dipolar Cycloaddition Chemistry; Wiley: New York, 1984; Vol. 1.

4. Mechanism of 1,3-dipolar cycloadditions. Reply

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