Аннотация:
Substituted 1-methyl-3,4-dihydrobenzo[f]isoquinoline interacts with substituted 5-methoxycarbonyl-2,3-dihydro-2,3-pyrrolediones to give substituted 1-oxo-1,2,10,11-tetrahydrobenzo[h]pyrrolo[2,1-a]isoquinoline-2-spiro-2-(4-hydroxy-5-oxo-2,5-dihydropyrroles).
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Yu. N. Bannikova, A. N. Maslivets, Yu. S. Rozhkova, Z. G. Aliev, “Spiro heterocyclization of 5-methoxycarbonyl-2,3-dihydro-2,3-pyrrolediones by reaction with 1-methyl-3,4-dihydroisoquinoline”, Mendeleev Commun., 15:4 (2005), 158–159
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3726
https://www.mathnet.ru/rus/mendc/v15/i4/p158
Эта публикация цитируется в следующих 9 статьяx:
Valeriya V. Konovalova, Andrey N. Maslivets, “Synthesis of Spiro Compounds Based on 1H-Pyrrole-2,3-Diones”, MROC, 16:2 (2019), 173
Vladimir E. Zhulanov, Maksim V. Dmitriev, Andrey N. Maslivets, Michael Rubin, “New method for in situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions”, RSC Adv., 6:93 (2016), 90239
Alexey Yu. Dubovtsev, Pavel S. Silaichev, Mikhail A. Nazarov, Maksim V. Dmitriev, Andrey N. Maslivets, Michael Rubin, “Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines”, RSC Adv., 6:88 (2016), 84730
Pavel Silaichev, Valeriy Filimonov, Pavel Slepukhin, Аndrey Maslivets, “Spiroheterocyclization of Methyl 1-Aryl-3-cinnamoyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates by the Action of 3-(Arylamino)-1H-inden-1-ones”, Molecules, 17:12 (2012), 13787
E. S. Denislamova, A. N. Maslivets, “Five-membered 2.3-dioxo heterocycles: LXVIII. Three pathways in the reaction of methyl 3-aroyl-1-aryl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with 3-amino-5,5-dimethylcyclohex-2-en-1-one”, Russ J Org Chem, 46:3 (2010), 389
Yuchen Tang, James C. Fettinger, Jared T. Shaw, “One-Step Synthesis of Complex Nitrogen Heterocycles from Imines and Alkyl-Substituted Maleic Anhydrides”, Org. Lett., 11:17 (2009), 3802
N. L. Racheva, Yu. V. Shklyaev, Yu. S. Rozhkova, A. N. Maslivets, “Five-membered 2,3-dioxo heterocycles: LIII. Reaction of 3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with substituted 1,3,3-trimethyl-3,4-dihydroisoquinolines. A new approach to 13-aza analogs of steroids”, Russ J Org Chem, 43:9 (2007), 1330
Yu. N. Bannikova, E. A. Sedegova, V. V. Khalturina, A. N. Maslivets, “Five-membered 2,3-dioxo heterocycles: LV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with ethyl 3-arylaminobut-2-enoates”, Russ J Org Chem, 43:9 (2007), 1338
Yuliya N. Bannikova, Andrei N. Maslivets, Yuliya S. Rozhkova, Yurii V. Shklyaev, Zainutdin G. Aliev, “Spiro Heterocyclization of 5‐Methoxycarbonyl‐2,3‐dihydro‐2,3‐pyrrolediones by Reaction with 1‐Methyl‐3,4‐dihydroisoquinoline.”, ChemInform, 36:45 (2005)
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