Synthesis, Table of Contents PAPER© Georg Thieme Verlag Stuttgart ˙ New YorkMicrowave-Assisted Synthesis and Functionalization of SelenolopyrimidinesStéphanie Hesse*, Célia Chenet, David Thomae, Gilbert KirschLaboratoire d’Ingénierie Moléculaire et Biochimie Pharmacologique, Institut Jean Barriol FR CNRS 2843, Université Paul Verlaine-Metz, 1 Boulevard Arago, 57070 Metz, FranceFax: +33(3)87315801; e-Mail: hesse@univ-metz.fr; Recommend Article Abstract Buy Article(opens in new window) All articles of this category(opens in new window) Abstract Microwave-assisted synthesis allowed efficient access to 4-chloroselenolo[3,2-d]pyrimidines in short times and very good yields. Some functionalizations by SNAr and palladium-catalyzed reactions are also reported. Key words selenium - pyrimidines - heterocycles - cyclizations - microwave-assisted reactions Full Text References References <A NAME="RZ25308SS-1">1</A> Gangjee A. Namjoshi OA. Yu J. Ihnat MA. Thorpe JE. Warnke LA. Bioorg. Med. Chem. 2008, 16: 5514 <A NAME="RZ25308SS-2">2</A> Ducray R. Ballard P. Barlaam BC. Hickinson MD. Kettle JG. Ogilvie DJ. Trigwell CB. Bioorg. Med. Chem. Lett. 2008, 18: 959 <A NAME="RZ25308SS-3">3</A> Gillespie RJ. Adams DR. Bebbington D. Benwell K. Cliffe IA. Dawson CE. Dourish CT. Fletcher A. Gaur S. Giles P. Jordan AM. Knight AR. Knutsen LJS. Lawrence A. Lerpiniere J. Misra A. Porter RHP. Pratt RM. Shepherd R. Upton R. Ward SE. Weiss SM. Williamson DS. Bioorg. Med. Chem. Lett. 2008, 18: 2916 <A NAME="RZ25308SS-4">4</A> DiMauro EF. Newcomb J. Nunes JJ. Bemis JE. Boucher C. Buchanan JL. Buckner WH. Cheng A. Faust T. Hsieh F. Huang X. Lee JH. Marshall TL. Martin MW. McGowan DC. Schneider S. Turci SM. White RD. Zhu X. Bioorg. Med. Chem. Lett. 2007, 17: 2305 <A NAME="RZ25308SS-5A">5a</A> Litivinov VP. Mortikov VY. Synthesis 1985, 98 <A NAME="RZ25308SS-5B">5b</A> Nandeeshaiah SK. Ambekar SY. Synth. Commun. 1995, 25: 451 <A NAME="RZ25308SS-5C">5c</A> Abdel-Hafez ShH. Russ. J. Org. Chem. 2005, 41: 396 <A NAME="RZ25308SS-5D">5d</A> Abdel-Hafez ShH. Abdel-Mohsen SH. El-Ossailly YA. Phosphorus, Sulfur Silicon Relat. Elem. 2006, 181: 2297 <A NAME="RZ25308SS-6A">6a</A> Sommen G. Comel A. Kirsch G. Synlett 2003, 855 <A NAME="RZ25308SS-6B">6b</A> Sommen G. Comel A. Kirsch G. Synthesis 2004, 451 <A NAME="RZ25308SS-7">7</A> Thomae D. Kirsch G. Seck P. Synthesis 2008, 1600 <A NAME="RZ25308SS-8">8</A> Hesse S. Perspicace E. Kirsch G. Tetrahedron Lett. 2007, 48: 5261 <A NAME="RZ25308SS-9A">9a</A> Gopal M. Veeranna S. Doddamani LS. Spectrosc. Lett. 2004, 37: 347 <A NAME="RZ25308SS-9B">9b</A> Gopal M. Veeranna S. J. Photochem. Photobiol., B 2005, 81: 181 <A NAME="RZ25308SS-10">10</A> Abdel-Hafez ShH. Eur. J. Med. Chem. 2008, 9: 1971 <A NAME="RZ25308SS-11A">11a</A> Mason JJ. Bergman J. Org. Biomol. Chem. 2007, 5: 2486 <A NAME="RZ25308SS-11B">11b</A> Zhou H.-B. Liu G.-S. Yao Z.-J. J. Org. Chem. 2007, 72: 6270 ; and references cited therein