| Autor: |
Mochalov, S. S., Gazzaeva, R. A., Fedotov, A. N., Archegov, B. P., Trofimova, E. V., Shabarov, Yu. S., Zefirov, N. S. |
| Předmět: |
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| Zdroj: |
Russian Journal of Organic Chemistry; Mar2005, Vol. 41 Issue 3, p406-416, 11p |
| Abstrakt: |
Electrophilic nitration of benzylcyclopropanes, allylbenzenes, and diphenylmethanes containing ortho, para-orienting substituents in the para position of the benzene ring results mainly in replacement of the cyclopropylmethyl, allyl, or benzyl group, respectively ( ipso substitution). The nitration of 4-cyclopropylallylbenzene is not accompanied by nitrodealkylation, and the products are only 2- and 3-nitro-4-cyclopropylallylbenzenes. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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