References
- Migianu , E. and Kirsch , G. 2002 . Synthesis of new thieno [b] azepinediones from α‐methylene ketones . Synthesis , 8 : 1096
- Kunick , C. , Schultz , C. , Lemcke , T. , Zaharevitz , D. W. , Gussio , R. , Jalluri , R. K. , Sausville , E. A. , Leost , M. and Meijer , L. 2000 . 2‐Substituted paullones: CDK1/cyclin B‐inhibiting property and in vitro antiproliferative activity . Bioorg. Med. Chem Lett. , 10 : 567 For instance, new thieno analogues of kenpaullones and pyrimidines have been reported to possess medicinal and biological activity
- Kunick , C. , Lauenroth , K. , Leost , M. , Meijer , L. and Lemcke , T. 2004 . 1‐Azakenpaullone is a selective inhibitor of glycogen synthase kinase‐3β . Bioorg. Med. Chem. Lett. , 14 : 413
- Brault , L. , Migianu , E. , Neguesque , A. , Battaglia , E. , Bagrese , D. and Kirsch , G. 2005 . New thiophene analogues of kenpaullone: synthesis and biological evaluation in breast cancer cells . Eur. J. Med. Chem. , 40 : 757
- Mohan , C. , Singh Parvesh , S. and Mahajan , M. P. 2005 . Tetrahedron , 61 : 10774
- Crespo , M. , Pagès , L. , Vega , A. , Segarra , M. , Lopez , M. , Doménech , T. , Miralpeix , M. , Beleta , J. , Ryder , H. and Palacios , J. 1998 . J. Design, synthesis, and biological activities of new [3, 2‐d] pyrimidines as selective type 4 phosphodiesterase inhibitors . J. Med. Chem. , 41 : 4021
- Dijkstra , D. and Backer , J. 1954 . Properties of the sulfonyl group: α‐substituted methyl sulfonylacetonitriles . Rec. Trav. Chim. Pays Bas. , 73 : 569
- Pochat , F. 1979 . Voie d'accès aux cétonitriles α‐thioéthers R‐CO‐CH(SEt)‐CN à partir des thioéthers R[dbnd]CH[dbnd](SEt)‐CN . Tetrahedron Lett. , 20 : 19
- Kowalski , P. , Mitka , K. , Ossowska , K. and Kolarka , Z. 2005 . Oxidation of sulfides to sulfoxides, part 1: Oxidation using halogen derivatives . Tetrahedron , 61 : 1948