Аннотация:
1-Alkylamino-5,5-dimethyl-1-cyclohexen-3-ones react with pyrrolo[1,2-a]quinoxaline-1,2,4-triones to form substituted 3,10,13-triazapentacyclo[10.7.1.01,10.04,9.014,19]icosa-4,6,8,14(19)-tetraene-2,11,18-triones.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
K. S. Bozdyreva, A. N. Maslivets, Z. G. Aliev, “Nucleophilic [3 + 3] addition of dimedone N-alkylimines to pyrrolo[1,2-a]quinoxaline-1,2,4-triones”, Mendeleev Commun., 15:4 (2005), 163–164
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3729
https://www.mathnet.ru/rus/mendc/v15/i4/p163
Эта публикация цитируется в следующих 10 статьяx:
N. A. Tretyakov, M. V. Dmitriev, A. N. Maslivets, “Reaction of Pyrrolo[2,1-c][1,4]oxazine-1,6,7-triones with 3-(Arylamino)-5,5-dimethylcyclohex-2-en-1-ones. Synthesis of Spiro[indole-3,2′-pyrroles]”, Russ J Org Chem, 57:1 (2021), 13
P. A. Topanov, I. V. Mashevskaya, M. V. Dmitriev, A. N. Maslivets, “Nucleophilic Addition of Oxindole to
Pyrroloquinoxalinetriones”, Russ J Org Chem, 56:4 (2020), 719
N. A. Tretyakov, A. N. Maslivets, “Reaction of Pyrrolo[2,1-a][1,4]oxazine-1,6,7-triones with Carbocyclic Enamino Ketones. Synthesis of Spiro[indole-3,2′-pyrroles]”, Russ J Org Chem, 55:10 (2019), 1618
A. V. Chervyakov, M. V. Dmitriev, A. N. Maslivets, “Synthesis of Spiro[indole-3,2′-pyrroles] from Pyrrolopyrazinetriones and Aminocyclohexenones”, Russ J Org Chem, 54:6 (2018), 951
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
V. V. Konovalova, Yu. V. Shklyaev, A. N. Maslivets, “Reaction of 3-aroylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones with quinaldine and substituted quinoxalines”, Russ J Org Chem, 51:5 (2015), 680
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
El Sayed H. El Ashry, Laila F. Awad, Yeldez El Kilany, Elsayed I. Ibrahim, Advances in Heterocyclic Chemistry, 98, Advances in Heterocyclic Chemistry Volume 98, 2009, 1
K. S. Bozdyreva, Z. G. Aliev, A. N. Maslivets, “Five-membered 2,3-dioxo heterocycles: LVII. Recyclization of 3-pivaloylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones by the action of o-phenylenediamine. Crystalline and molecular structure of 3-[3,3-dimethyl-2-oxo-1-(3-oxo-3,4-dihydroquinoxalin-2-yl)butyl]-1-phenylquinoxalin-2(1H)-one”, Russ J Org Chem, 44:4 (2008), 607
Ksenia S. Bozdyreva, Andrei N. Maslivets, Zainutdin G. Aliev, “Nucleophilic [3 + 3] Addition of Dimedone N‐Alkylimines to Pyrrolo[1,2‐a]quinoxaline‐1,2,4‐triones”, ChemInform, 36:44 (2005)
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