Dipolar cycloaddition reactions of organic azides with some acetylenic compounds
ST Abu??Orabi, MA Atfah, I Jibril…
Index: Abu-Orabi, Sultan T.; Atfah, M. Adnan; Jibril, Ibrahim; Mari'i, Fakhri M.; Ali, Amer Al-Sheikh Journal of Heterocyclic Chemistry, 1989 , vol. 26, p. 1461 - 1468
Full Text: HTML
Citation Number: 126
Abstract
Abstract Phenyl azide 1 and several substituted benzyl azides 2a-o underwent 1, 3-dipolar cycloaddition reactions with dimethyl acetylenedicarboxylate 3, phenylacetylene 4 and ethyl propiolate 5 to afford the triazoles 6-13. The reactions of these azides with ethyl propiolate were found to be completely regiospecific.
Related Articles:
Per (2-thienyl) pyridines: Synthesis and Properties
[Potratz, Stefanie; Mishra, Amaresh; Baeuerle, Peter Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 683 - 692]
[Alonso, Francisco; Moglie, Yanina; Radivoy, Gabriel; Yus, Miguel Advanced Synthesis and Catalysis, 2010 , vol. 352, # 18 p. 3208 - 3214]
Per (2-thienyl) pyridines: Synthesis and Properties
[Potratz, Stefanie; Mishra, Amaresh; Baeuerle, Peter Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 683 - 692]
[Bedford, C. D.; Bruckmann, E. M.; Smith, P. A. S. Journal of Organic Chemistry, 1981 , vol. 46, # 4 p. 679 - 686]
[Oetvoes, Sandor B.; Mandity, Istvan M.; Kiss, Lorand; Fueloep, Ferenc Chemistry - An Asian Journal, 2013 , vol. 8, # 4 p. 800 - 808]