Synthesis and study of L-arabinopyranosides of 5- and 6-nitroindoles

Autor:	I. V. Yartseva, M. N. Preobrazhenskaya, V. I. Mukhanov, L. V. Ektova, T. D. Miniker, N. D. Chkanikov
Rok vydání:	1979
Předmět:	Indole test Acetylation Chemistry Organic Chemistry Condensation Amino derivatives Organic chemistry Dehydrogenation
Zdroj:	Chemistry of Heterocyclic Compounds. 15:188-193
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00480365
Popis:	Condensation of 5- or 6-nitroindoline with L-arabinose gave 1-α-L-arabinopyranosyl-5 (or 6)-nitroindolines, which, after acetylation, dehydrogenation, and removal of the protective groups, are converted to 1-α-L-arabinopyranosyl-5(or 6)-nitroindoles and then to the corresponding amino derivatives. 1-α-L-Arabinopyranosyl-6-nitro-3-bromo-(iodo)indoles were obtained. The selective 2′-O- and 3′-O-deacetylation of 1-(2′, 3′, 4′-tri-O-acetyl)-α-L-arabinopyranosyl-6-nitroindole was accomplished.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::106edd4a31f29f6ca31855373e76a8fa https://doi.org/10.1007/bf00480365 Zobrazit plný text záznamu Full text from SpringerLink