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Reaction of synthetic equivalents of arylideneimines , viz
| Content Provider | Semantic Scholar |
|---|---|
| Author | Lozinskaya, Natalia A. Sosonyuk, Sergey E. Firsova, Yu. N. Proskurnina, Marina V. Zefirov, Nikolai Serafimovich |
| Copyright Year | 2009 |
| Abstract | N,N ́ Bis(arylidene)methanediamines regiospecifically react with 2,3 diphenylcyclo propenone to form stable adducts of both the mono and the diaddition. Ammonium acetate serves as the catalyst of the process. During hydrolysis of these adducts, an oxidative coupling of 1,2 dihydro 3H pyrrol 3 ones occurs with the formation of 2,2 ́,4,4 ́,5,5 ́ hexaaryl 1,1 ́,2,2 ́ tetrahydro 3H,3 ́H 2,2 ́ bipyrrole 3,3 ́ diones. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | https://istina.msu.ru/download/74501375/1gXajf:rvgws3kl941Ql0Ud9tak0FMY7PY/ |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |