Аннотация:
2-Vinyl- and 2,7-divinyl-1,8-bis(dimethylamino)naphthalenes with strong –M substituents in the β-positions of vinyl groups have been shown to undergo a tert-amino-type rearrangement providing a new and facile route to benzo[h]quinoline and quino[7,8:7’,8’]quinoline derivatives.
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2983
https://www.mathnet.ru/rus/mendc/v20/i1/p36
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
Marina P. Vlasenko, Valery A. Ozeryanskii, “One‐scale basicities of diaminobenzenes and diaminonaphthalenes: from aniline to proton sponge”, J of Physical Organic Chem, 30:2 (2017)
A. Yu. Platonova, A. A. Poluikova, O. A. Trofimova, T. V. Glukhareva, Yu. Yu. Morzherin, “Microwave-Assisted Synthesis of Fused 3-Thiocarbamoylquinolines by Reinhoudt Reaction and their Modification by Hantzsch Reaction”, Chem Heterocycl Comp, 50:10 (2015), 1450
A. Yu. Platonova, A. A. Poluikova, T. V. Glukhareva, Yu. Yu. Morzherin, “Synthesis of fused 3-cyano- and 3-carbamoyl-1,2,3,4-tetrahydroquinolines”, Russ Chem Bull, 63:7 (2014), 1580
A. Yu. Platonova, T. V. Glukhareva, O. A. Zimovets, Yu. Yu. Morzherin, “tert-Amino effect: the Meth-Cohn and Reinhoudt reactions (Review)”, Chem Heterocycl Comp, 49:3 (2013), 357
Xuefeng Gao, Vikram Gaddam, Erich Altenhofer, Rama Rao Tata, Zhengxin Cai, Nattawut Yongpruksa, Aswin K. Garimallaprabhakaran, Michael Harmata, “CH Activation in S‐Alkenyl Sulfoximines: An Endo 1,5‐Hydrogen Migration”, Angew Chem Int Ed, 51:28 (2012), 7016
Xuefeng Gao, Vikram Gaddam, Erich Altenhofer, Rama Rao Tata, Zhengxin Cai, Nattawut Yongpruksa, Aswin K. Garimallaprabhakaran, Michael Harmata, “CH Activation in S‐Alkenyl Sulfoximines: An Endo 1,5‐Hydrogen Migration”, Angewandte Chemie, 124:28 (2012), 7122
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
Maria A. Povalyakhina, Alexander F. Pozharskii, Olga V. Dyablo, Valery A. Ozeryanskii, Oksana V. Ryabtosova, “ChemInform Abstract: tert‐Amino Effect in Naphthalene Proton Sponges: A Novel Approach to Benzo[h]quinoline and Quino[7,8:7′,8′]quinoline Derivatives.”, ChemInform, 41:25 (2010)