Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone / Ivanova Anna E.,Burgart Yanina V.,Saloutin Viktor I. // MENDELEEV COMMUNICATIONS. - 2016. - V. 26, l. 2. - P. 106-108.

ISSN/EISSN:

0959-9436 / 1364-551X

Type:

Article

Abstract:

Ribosylation of 4-aryldiazenyl-3-R-5-R'-pyrazoles with 1,2,3,5-tetra-O-acetyl-beta-D-ribofuranose in the presence of tin(IV) chloride gives alpha- and beta-anomeric N-(2,3,5-tri-O-acetylribofuranosyl)-substituted derivatives. Their HPLC separation and deacetylation (MeOH, MeONa) affords 1-(beta-D-ribofuranosyl)-3-R-5-R'-4-(aryldiazenyl)-1H-pyrazoles.

Author keywords:

нет данных

DOI:

10.1016/j.mencom.2016.03.006

Web of Science ID:

ISI:000374813300006

Соавторы в МНС:

Другие поля

Поле	Значение
Month	MAR-APR
Publisher	ELSEVIER SCIENCE BV
Address	PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
Language	English
EISSN	1364-551X
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	ivanova@ios.uran.ru
ResearcherID-Numbers	Burgart, Yanina/T-8025-2017
ORCID-Numbers	Burgart, Yanina/0000-0001-6061-2410
Funding-Acknowledgement	UB RAS {[}15-21-3-5]
Funding-Text	This study was supported by the project UB RAS (no. 15-21-3-5).
Number-of-Cited-References	11
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	2
Journal-ISO	Mendeleev Commun.
Doc-Delivery-Number	DK3JQ