Special features of 1,3-dipolar cycloaddition of n-methylazomethinylid to nitrobenzazoles
Chemistry of Heterocyclic Compounds, ISSN: 0009-3122, Vol: 47, Issue: 2, Page: 215-221
2011
- 12Citations
- 3Captures
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Article Description
Synthetic approaches to 1,3-dipolar cycloaddition of N-methylazomethinylid to mononitrobenzazole are described. The geometric and electronic structures have been studied by quantum chemical methods (HF/STO-3 G and B3LYP/6-31 G) and the reactivity indexes of compounds have been estimated. It was shown that 1,3-dipolar cycloaddition of N-methylazomethinylid to the dipolarophile has a polar character and proceeds in accordance with the normal (noninversion) electronic distribution. © 2011 Springer Science+Business Media, Inc.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=80052605857&origin=inward; http://dx.doi.org/10.1007/s10593-011-0743-y; http://link.springer.com/10.1007/s10593-011-0743-y; https://dx.doi.org/10.1007/s10593-011-0743-y; https://link.springer.com/article/10.1007/s10593-011-0743-y; http://www.springerlink.com/index/10.1007/s10593-011-0743-y; http://www.springerlink.com/index/pdf/10.1007/s10593-011-0743-y
Springer Science and Business Media LLC
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