Аннотация:
Using glaucine as an example, a convenient access to naphtho[2,1-f]isoquinoline (litebamine) derivatives is proposed. The synthetic scheme involves a stepwise pyridine–pyridine recyclization of the intermediate N-acylsecoaporphine analogues.
Образец цитирования:
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, L. G. Kuz'mina, G. S. Borodkin, A. I. Klimenko, “Recyclization of glaucine as a new route to litebamine derivatives”, Mendeleev Commun., 28:1 (2018), 58–60
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1663
https://www.mathnet.ru/rus/mendc/v28/i1/p58
Эта публикация цитируется в следующих 8 статьяx:
S. S. Khizrieva, S. N. Borisenko, E. V. Maksimenko, E. V. Vetrova, N. I. Borisenko, V. I. Minkin, “Antioxidant Properties and Effects of Aporphine Alkaloids and Their Phenanthrene Seco-Isomers on Acetylcholinesterase Activity”, Russ J Bioorg Chem, 48:7 (2022), 1433
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. S. Sochnev, O. P. Demidov, A. N. Bodryakov, L. N. Fetisov, K. N. Kononenko, M. A. Bodryakova, A. I. Klimenko, “New Azepine-Furan Spirocyclic Structures in the Reaction of
4-Aroyl-1,2-dihydrobenzo[d]azepines and
2-Aroyl-4,5-dihydrophenanthreno[1,2-d]azepine
with Formaldehyde”, Russ J Gen Chem, 91:5 (2021), 792
Salima Salimovna Khizrieva, Sergey Nikolaevich Borisenko, Elena Vladimirovna Maksimenko, Elena Vladimirovna Vetrova, Nikolay Ivanovich Borisenko, Vladimir Isaakovich Minkin, “ANTIOXIDANT PROPERTIES AND EFFECTS OF APORPHINE ALKALOIDS AND THEIR PHENANTHRENE SECO-ISOMERS ON ACETYLCHOLINESTERASE ACTIVITY”, JCPRM, 2021, no. 2, 237
A. A. Zubenko, V. S. Sochnev, V. G. Kartsev, L. N. Divaeva, O. P. Demidov, A. I. Klimenko, A. N. Bodryakov, M. A. Bodryakova, G. S. Borodkin, A. S. Morkovnik, “Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion”, Mendeleev Commun., 31:4 (2021), 545–547
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, O. P. Demidov, V. S. Sochnev, I. G. Borodkina, Yu. D. Drobin, A. A. Spasov, “New route to bioactive 2-(hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3-dihydroazepines”, Mendeleev Commun., 30:1 (2020), 28–30
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, A. A. Anisimov, K. Yu. Suponitsky, “Pyridine—Azepine Structural Modification of 3,4-Dihydro-nor-isoharmine”, Russ J Org Chem, 55:1 (2019), 74
A. A. Zubenko, L. N. Divaeva, A. S. Morkovnik, V. G. Kartsev, Y. D. Drobin, N. M. Serbinovskaya, L. N. Fetisov, A. N. Bodryakov, M. A. Bodryakova, L. A. Lyashenko, A. I. Klimenko, “Synthesis and Anti-Infective Activity of 2-Heteroaryl(Acyl)-9,10,12,13-Tetramethoxy-3-Methyl-4,5-Dihydro-3H-Phenanthro[1,2-d]Azepines”, Russ J Bioorg Chem, 44:4 (2018), 461
A. A. Zubenko, A. S. Morkovnik, L. N. Divaeva, V. G. Kartsev, K. Yu. Suponitsky, A. I. Klimenko, “Synthesis of phenanthro[1,2-d]azepine derivatives containing a new heterocyclic system from the aporphine alkaloid glaucine”, Mendeleev Commun., 28:3 (2018), 320–322