Non-natural nucleosides based on 1,2,4-triazolo{[}5,1-c]{[}1,2,4]triazin-4(6H)-ones / Deev Sergey L.,Shestakova Tatiana S.,Rusinov Vladimir L.,Chupakhin Oleg N.,Shashkov Alexander S. // ARKIVOC. - 2009. - V. , l. . - P. 196-207.

ISSN/EISSN:

1424-6376 / нет данных

Type:

Article

Abstract:

Two regioselective methods for the synthesis of nucleosides in the series of 3-phenyl- and 3-ethoxycarbonyl-1,2,4-triazolo{[}5,1-c]{[}1,2,4]triazin-4-ones were developed. The first route involves a Vorbruggen glycosylation reaction. The second one is based on condensation of 1,2,4-triazolo{[}5,1-c]{[}1,2,4]triazin-4-one sodium salts with protected 1-bromo-sugar derivatives.

Author keywords:

1,2,4-Triazolo{[}5,1-c]{[}1,2,4]triazin-4-ones; glycosylation; NMR spectra; beta-configuration; X-ray INHIBITORS; STRATEGIES

DOI:

нет данных

Web of Science ID:

ISI:000266695800021

Соавторы в МНС:

Другие поля

Поле	Значение
Publisher	ARKAT USA INC
Address	C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA
Language	English
Keywords-Plus	INHIBITORS; STRATEGIES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	chupakhin@ios.uran.ru
Number-of-Cited-References	21
Usage-Count-Since-2013	1
Journal-ISO	Arkivoc
Doc-Delivery-Number	454PW