Synthesis of acyclic nucleotide analogues derived from 2-amino-6-.I.C./I.-substituted purines .I.via./I. cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl}-6-halopurines with diverse organometallic reagents

0193803 - UOCHB-X 20000235 RIV CZ eng J - Journal Article
Česnek, Michal - Hocek, Michal - Holý, Antonín
Synthesis of acyclic nucleotide analogues derived from 2-amino-6-.I.C./I.-substituted purines .I.via./I. cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl}-6-halopurines with diverse organometallic reagents.
Collection of Czechoslovak Chemical Communications. Roč. 65, č. 8 (2000), s. 1357-1373. ISSN 0010-0765
R&D Projects: GA ČR GA203/98/P027; GA ČR GV203/96/K001; GA AV ČR KSK2055603
Institutional research plan: CEZ:AV0Z4055905
Subject RIV: CC - Organic Chemistry
Impact factor: 0.960, year: 2000

Acyclic nucleotide analogues derived from 2-amino-6-C-substituted purines were prepared by cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl}-6-halopurines with organometallic reagents.
Permanent Link: http://hdl.handle.net/11104/0089495