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Mendeleev Communications, 2019, Volume 29, Issue 1, Pages 53–54
DOI: https://doi.org/10.1016/j.mencom.2019.01.016
(Mi mendc1418)
 

This article is cited in 2 scientific papers (total in 2 papers)

Communications

1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene

A. B. Budaeva, A. V. Ivanova, O. V. Petrovaa, V. A. Samsonovb, I. A. Ushakova, A. Ya. Tikhonovb, L. N. Sobeninaa, B. A. Trofimova

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract: 6,7-Dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime is annelated with acetylene in the KOH/DMSO/H2O system under pressure to give NH- or N-vinyl-5,8-dihydro-4H-[1,2,5]oxadiazolo[3,4-g]indoles in 29 and 68% yields, respectively. These derivatives are readily aromatized with DDQ at room temperature to the expected indoles.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (143.7 Kb)


Citation: A. B. Budaev, A. V. Ivanov, O. V. Petrova, V. A. Samsonov, I. A. Ushakov, A. Ya. Tikhonov, L. N. Sobenina, B. A. Trofimov, “1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene”, Mendeleev Commun., 29:1 (2019), 53–54
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  • https://www.mathnet.ru/eng/mendc/v29/i1/p53
  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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