V. V. Lipson, S. M. Desenko, O. V. Shishkin, “Heterocyclization of 6-hydroxyimino-6,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidines into 1,2,4-triazolo[1,5-a]pyrimido[5,4-b]- and -[5,6-b]indoles”, Mendeleev Commun., 16:5 (2006), 280

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Mendeleev Communications, 2006, Volume 16, Issue 5, Pages 280–282
DOI: https://doi.org/10.1070/MC2006v016n05ABEH002361 (Mi mendc3624)

This article is cited in 8 scientific papers (total in 8 papers)

Heterocyclization of 6-hydroxyimino-6,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidines into 1,2,4-triazolo[1,5-a]pyrimido[5,4-b]- and -[5,6-b]indoles

V. V. Lipson^a, S. M. Desenko^b, O. V. Shishkin^b

^a V.Ya. Danilevsky Institute of Endocrine Pathology Problems, Kharkov, Ukraine
^b STC 'Institute for Single Crystals', National Academy of Sciences of Ukraine, Kharkov, Ukraine

Full-text PDF (216 kB) Citations (8)

DOI: https://doi.org/10.1070/MC2006v016n05ABEH002361

Abstract: 6-Hydroxyimino-6,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidines are converted into isomeric 1,2,4-triazolo[1,5-a]pyrimido[5,4-b]- and -[5,6-b]indoles in polyphosphoric acid or under exposure to para-nitrobenzoyl chloride in pyridine.

Bibliographic databases:

Document Type: Article

Language: English

Citation: V. V. Lipson, S. M. Desenko, O. V. Shishkin, “Heterocyclization of 6-hydroxyimino-6,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidines into 1,2,4-triazolo[1,5-a]pyrimido[5,4-b]- and -[5,6-b]indoles”, Mendeleev Commun., 16:5 (2006), 280–282

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https://www.mathnet.ru/eng/mendc/v16/i5/p280

This publication is cited in the following 8 articles:

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