Volume 31, Issue 7
Natural Products
Full Access

ChemInform Abstract: Regioselective N1-Alkylation of Guanosine Derivatives Protected at N2 by an N,N-Dialkyl Amidine Group.

Stephane P. Vincent

Stephane P. Vincent

Lab. Synth. Bio-Org., CNRS, Fac. Pharm., Univ. Louis Pasteur, F-67401 Illkirch, Fr.

Search for more papers by this author
Charles Mioskowski

Charles Mioskowski

Lab. Synth. Bio-Org., CNRS, Fac. Pharm., Univ. Louis Pasteur, F-67401 Illkirch, Fr.

Search for more papers by this author
Luc Lebeau

Luc Lebeau

Lab. Synth. Bio-Org., CNRS, Fac. Pharm., Univ. Louis Pasteur, F-67401 Illkirch, Fr.

Search for more papers by this author
First published: 10 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

Under Mitsunobu conditions or in the presence of electrophilic alkylating reagents, alkylation of guanosine derivatives (I) and (IV), protected by an N,N-dialkyl amidine at the exocyclic amino group, occurs selectively on nitrogen N1 of the purine base.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.