z-logo
Premium
Regioselective Synthesis and Antiviral Activity of Purine Nucleoside Analogues with Acyclic Substituents at N7
Author(s) -
Jähne Gerhard,
Kroha Herbert,
Müller Armin,
Helsberg Matthias,
Winkler Irvin,
Gross Gerhard,
Scholl Thomas
Publication year - 1994
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199405621
Subject(s) - purine , regioselectivity , substituent , chemistry , stereochemistry , residue (chemistry) , nucleoside , derivative (finance) , combinatorial chemistry , biochemistry , enzyme , catalysis , financial economics , economics
A new class of antiviral compounds is heralded by purine derivative 1 , which in vitro tests showed to have good antiherpes action. This compound proves that, like the natural purine nucleosides with a cyclic residue at N9, derivatives with an acyclic substituent at N7 can also be active.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here