NMR Study of the Tautomeric Behavior of N-(α-Aminoalkyl)tetrazoles-Reference-Cited by-同舟云学术

NMR Study of the Tautomeric Behavior of N-(α-Aminoalkyl)tetrazoles

Published:2010-09-09 Issue:19 Volume:75 Page:6468-6476
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Katritzky Alan R.¹,El-Gendy Bahaa El-Dien M.¹²,Draghici Bogdan¹,Hall C. Dennis¹,Steel Peter J.³

Affiliation:

1. Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200

2. Department of Chemistry, Faculty of Science, Benha University, Benha, Egypt

3. Chemistry Department, University of Canterbury, Christchurch 8140, New Zealand

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101195z

Reference38 articles.

1. Butler, R. N.InComprehensive Heterocyclic Chemistry II;Katritzky, A. R., Rees, C. W., Scriven, E. F. V., Eds.Elsevier:Oxford, U.K., 1996; Vol.4, pp621−678.

2. 4 Medicinal Chemistry of Tetrazoles

3. Recent Advances in Tetrazole Chemistry

4. cBenson, F. R.InHeterocyclic Compounds;Elderfield, R. C., Eds.Wiley:New York, 1968; Vol.8, pp1−104.

5. Tetrazoles are Potent Anion Recognition Elements That Emulate the Disfavored Anti Conformations of Carboxylic Acids

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