Synthesis of 1-?-D-ribopyranosyl- and ribofuranosyl-6-nitroindole and indoline for the phosphotriester oligonucleotide synthesis

Autor:	Sh. A. Samsoniya, M. O. Taktakishvili, M. N. Preobrazhenskaya, T. K. Tsitskishvili, V. S. Kikoladze
Rok vydání:	1990
Předmět:	chemistry.chemical_compound Glycosylation chemistry Organic Chemistry Indoline Dehydrogenation Oligonucleotide synthesis Combinatorial chemistry
Zdroj:	Chemistry of Heterocyclic Compounds. 26:1249-1254
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00476979
Popis:	The glycosylation reaction of 6-nitroindoline with 5-tritylribose led to the synthesis of the 1-Β-D-ribofuranoside and 1-Β-D-ribopyranoside of 6-nitroindoline, the dehydrogenation of which resulted in the isolation of the corresponding 1-Β-D-ribopyranoside and 1-Β-D-ribofuranoside of 6-nitroindole; the last with protecting groups are suitable for utilization in oligonucleotide synthesis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::473e4829bf0c238d8aa3bc64d1cf36c3 https://doi.org/10.1007/bf00476979 Zobrazit plný text záznamu Full text from SpringerLink