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Mendeleev Communications, 2004, Volume 14, Issue 2, Pages 75–76
DOI: https://doi.org/10.1070/MC2004v014n02ABEH001897
(Mi mendc3813)
 

This article is cited in 10 scientific papers (total in 10 papers)

Spiro heterocyclization of pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones under the action of 1,3,3-trimethyl-3,4-dihydroisoquinoline

I. V. Mashevskayaa, A. V. Duvalova, Yu. S. Rozhkovab, Yu. V. Shklyaevb, N. L. Rachevaa, K. S. Bozdyrevaa, A. N. Maslivetsa

a Department of Chemistry, Perm State National Research University, Perm, Russian Federation
b Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
Full-text PDF (88 kB) Citations (10)
Abstract: 1,3,3-Trimethyl-3,4-dihydroisoquinoline reacts with pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones to give substituted pyrrolo[2,1-a]-isoquinoline-2-spiro-2-pyrroles.
Document Type: Article
Language: English


Citation: I. V. Mashevskaya, A. V. Duvalov, Yu. S. Rozhkova, Yu. V. Shklyaev, N. L. Racheva, K. S. Bozdyreva, A. N. Maslivets, “Spiro heterocyclization of pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones under the action of 1,3,3-trimethyl-3,4-dihydroisoquinoline”, Mendeleev Commun., 14:2 (2004), 75–76
Linking options:
  • https://www.mathnet.ru/eng/mendc3813
  • https://www.mathnet.ru/eng/mendc/v14/i2/p75
  • This publication is cited in the following 10 articles:
    1. 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  crossref
    2. A. I. Kobelev, M. V. Dmitriev, A. N. Maslivets, “Reaction of Hetareno[e]pyrrolediones with 1,3-C,N-Binucleophiles. Isolation of Intermediate Product of Spiro Heterocyclization”, Russ J Org Chem, 56:7 (2020), 1321  crossref
    3. Valeriya V. Konovalova, Andrey N. Maslivets, “Synthesis of Spiro Compounds Based on 1H-Pyrrole-2,3-Diones”, MROC, 16:2 (2019), 173  crossref
    4. 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  crossref
    5. A. A. Maslivets, A. N. Maslivets, “Cascade spiro-heterocyclization of pyrrolo[1,2-a][4,1]-benzoxazepinetriones under the action of carbocyclic enaminoketones”, Russ J Org Chem, 51:8 (2015), 1194  crossref
    6. V. V. Konovalova, A. V. Kharitonova, Yu. V. Shklyaev, A. N. Maslivets, “Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with substituted acetamides of 3,4-dihydroisoquinolines”, Russ J Org Chem, 51:11 (2015), 1566  crossref
    7. 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  crossref
    8. 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  crossref
    9. 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  mathnet  crossref
    10. Irina V. Mashevskaya, Aleksei V. Duvalov, Yuliya S. Rozhkova, Yurii V. Shklyaev, Nadezhda L. Racheva, Kseniya S. Bozdyreva, Andrei N. Maslivets, “Spiro Heterocyclization of Pyrrolo[2,1‐c][1,4]benzoxazine‐1,2,4‐triones under the Action of 1,3,3‐Trimethyl‐3,4‐dihydroisoquinoline.”, ChemInform, 35:37 (2004)  crossref
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