Аннотация:
α-Phenylated 1,8-bis(dimethylamino)-2-naphthylmethyl carbocations have been shown to rearrange into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium cations through an intramolecular hydride shift from the 1-NMe2 group.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
O. V. Ryabtsova, A. F. Pozharskii, A. V. Degtyarev, V. A. Ozeryanskii, “Rearrangement of carbocations derived from 1,8-bis(dimethylamino)naphthyl-2-methanols into 4-R-1,1,3-trimethyl-2,3-dihydroperimidinium salts”, Mendeleev Commun., 16:6 (2006), 313–316
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3639
https://www.mathnet.ru/rus/mendc/v16/i6/p313
Эта публикация цитируется в следующих 10 статьяx:
Alexander F. Pozharskii, Anna V. Gulevskaya, Rosa M. Claramunt, Ibon Alkorta, José Elguero, “Perimidines: a unique π-amphoteric heteroaromatic system”, Усп. хим., 89:11 (2020), 1204–1260; Alexander F. Pozharskii, Anna V. Gulevskaya, Rosa M. Claramunt, Ibon Alkorta, José Elguero, “Perimidines: a unique π-amphoteric heteroaromatic system”, Russian Chem. Reviews, 89:11 (2020), 1204–1260
Valery A. Ozeryanskii, Anastasia Yu. Gorbacheva, Alexander F. Pozharskii, Marina P. Vlasenko, Alexander Yu. Tereznikov, Margarita S. Chernov'yants, “The first proton sponge-based amino acids: synthesis, acid–base properties and some reactivity”, Org. Biomol. Chem., 13:31 (2015), 8524
A. F. Pozharskii, V. A. Ozeryanskii, “Proton Sponges and Hydrogen Transfer Phenomena”, Mendeleev Commun., 22:3 (2012), 117–124
Alexander F. Pozharskii, Maria A. Povalyakhina, Alexander V. Degtyarev, Oxana V. Ryabtsova, Valery A. Ozeryanskii, Olga V. Dyablo, Anna V. Tkachuk, Olga N. Kazheva, Anatolii N. Chekhlov, Oleg A. Dyachenko, “Naphthalene proton sponges as hydride donors: diverse appearances of the tert-amino-effect”, Org. Biomol. Chem., 9:6 (2011), 1887
A. Brandi, M. Gensini, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms · 2006, 2010, 451
Alexander F. Pozharskii, Alexander V. Degtyarev, Valery A. Ozeryanskii, Oksana V. Ryabtsova, Zoya A. Starikova, Gennadii S. Borodkin, “1,8,1′,8′-Tetrakis(dimethylamino)-2,2′-dinaphthylmethanols: DoubleIn/OutProton Sponges with Low-Barrier Hydrogen-Bond Switching”, J. Org. Chem., 75:14 (2010), 4706
M. A. Povalyakhina, A. F. Pozharskii, O. V. Dyablo, V. A. Ozeryanskii, O. V. Ryabtsova, “tert-Amino effect in naphthalene proton sponges: a novel approach to benzo[h]quinoline and quino[7,8:7',8']quinoline derivatives”, Mendeleev Commun., 20:1 (2010), 36–38
Chen Zhang, Sandip Murarka, Daniel Seidel, “Facile Formation of Cyclic Aminals through a Brønsted Acid-Promoted Redox Process”, J. Org. Chem., 74:1 (2009), 419
R. G. Kostyanovsky, A. F. Pozharskii, Yu. V. Nelyubina, K. A. Lyssenko, G. K. Kadorkina, A. V. Degtyarev, O. G. Nabiev, I. I. Chervin, “Absolute configuration of a chiral proton sponge”, Mendeleev Commun., 18:2 (2008), 86–87
Oksana V. Ryabtsova, Alexander F. Pozharskii, Alexander V. Degtyarev, Valery A. Ozeryanskii, “Rearrangement of Carbocations Derived from 1,8‐Bis(dimethylamino)naphthyl‐2‐methanols into 4‐R‐1,1,3‐Trimethyl‐2,3‐dihydroperimidinium Salts”, ChemInform, 38:20 (2007)