Аннотация:
Carbanions formed from malononitrile and ethyl cyanoacetate have been found to react with pyridinium salts via ring-opening to form 1,1,7,7-tetrasubstituted hepta-1,3,5-trienes.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. S. Kiselev, A. A. Gakh, A. V. Samet, V. V. Semenov, “Aromatic Ring Opening of Pyridinium Salts using Carbanions formed from Malononitrile and Ethyl Cyanoacetate”, Mendeleev Commun., 2:1 (1992), 25–26
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5379
https://www.mathnet.ru/rus/mendc/v2/i1/p25
Эта публикация цитируется в следующих 4 статьяx:
Karoline G. Primdahl, Åsmund Kaupang, Jong-Duk Park, Mohammad R. Seyedsayamdost, Jens M. J. Nolsøe, Marius Aursnes, “On the Structure of Thailandene A: Synthetic Examination of the Cryptic Natural Product Aided by a Theoretical Approach”, Synthesis, 54:07 (2022), 1733
Dmitry V. Osipov, Darya А. Rashchepkina, Alina А. Аrtemenko, Oleg P. Demidov, Vitaly А. Osyanin, “Nucleophilic Dearomatization of 3-nitrobenzofurans by the Action of 2-(1-arylethylidene)Malononitriles”, Chem Heterocycl Comp, 57:10 (2021), 996
Jens M. J. Nolsøe, Marius Aursnes, Jørn E. Tungen, Trond V. Hansen, “Dienals Derived from Pyridinium Salts and Their Subsequent Application in Natural Product Synthesis”, J. Org. Chem., 80:11 (2015), 5377
A. S. KISELEV, A. A. GAKH, A. V. SAMET, V. V. SEMENOV, “ChemInform Abstract: Aromatic Ring Opening of Pyridinium Salts Using Carbanions Formed from Malononitrile and Ethyl Cyanoacetate.”, ChemInform, 23:39 (1992)
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