Bromination at C-5 of Pyrimidine and C-8 of Purine Nucleosides with 1,3-Dibromo-5,5-dimethylhydantoin.

[1]  T. Jamison,et al.  Encyclopedia of Reagents for Organic Synthesis, Second Edition , 2009 .

[2]  Hisashi Yamamoto,et al.  Lewis acid catalyzed benzylic bromination. , 2008, Chemistry, an Asian journal.

[3]  L. Clima,et al.  Building‐Block Approach for the Straightforward Incorporation of a New FRET (Fluorescence‐Resonance‐Energy Transfer) System into Synthetic DNA , 2008 .

[4]  A. Alam 1,3-Dibromo-5,5-dimethylhydantoin , 2005 .

[5]  A. Alam,et al.  Simple, Extremely Fast, and High‐Yielding Oxidation of Thiols to Disulfides , 2005 .

[6]  Hideyuki Ito,et al.  Multi-functionalization of gallic acid towards improved synthesis of α- and β-DDB , 2005 .

[7]  K. L. Nagpal,et al.  Bromination of nucleosides , 2005, Experientia.

[8]  M. Zolfigol,et al.  1,3-Dibromo-5,5-Dimethylhydantoin [DBDMH] as an Efficient and Selective Agent for the Oxidation of Thiols to Disulfides in Solution or under Solvent-Free Conditions , 2004 .

[9]  L. Agrofoglio,et al.  Palladium-assisted routes to nucleosides. , 2003, Chemical reviews.

[10]  S. Virgil 1,3‐Dibromo‐5,5‐dimethylhydantoin , 2001 .

[11]  S. Tannenbaum,et al.  A novel nitration product formed during the reaction of peroxynitrite with 2',3',5'-tri-O-acetyl-7,8-dihydro-8-oxoguanosine: N-nitro-N'-[1-(2,3,5-tri-O-acetyl-beta-D-erythro-pentofuranosyl)- 2, 4-dioxoimidazolidin-5-ylidene]guanidine. , 2000, Chemical research in toxicology.

[12]  E. De Clercq,et al.  Potent and selective inhibition of varicella-zoster virus (VZV) by nucleoside analogues with an unusual bicyclic base. , 1999, Journal of medicinal chemistry.

[13]  C. Chassaing,et al.  1,3-Dibromo-5,5-dimethylhydantoin, a useful reagent for aromatic bromination , 1997 .

[14]  C. Burrows,et al.  Bromination of pyrimidines using bromide and monoperoxysulfate: A competition study between cytidine, uridine and thymidine , 1997 .

[15]  P. Bovonsombat,et al.  DIBROMANTIN AS A REAGENT FOR THE AROMATIC BROMINATION OF POLYALKYLBENZENES , 1995 .

[16]  O. Arrad,et al.  New Aspects on the Preparation of 1,3-Dibromo-5,5-dimethylhydantoin , 1995 .

[17]  Rakesh Kumar,et al.  A mild and efficient methodology for the synthesis of 5-halogeno uracil nucleosides that occurs via a 5-halogeno-6-azido-5,6-dihydro intermediate , 1994 .

[18]  S. Fujisaki,et al.  Halogenation Using N-Halogenocompounds. II. Acid Catalyzed Bromination of Aromatic Compounds with 1,3-Dibromo-5,5-dimethylhydantoin , 1994 .

[19]  K. Hoogsteen,et al.  N-Bromosuccinimide/Dibromodimethylhydantoin in aqueous base: A practical method for the bromination of activated benzoic acids , 1993 .

[20]  C. K. Chu,et al.  Nucleosides and Nucleotides as Antitumor and Antiviral Agents , 1993, Springer US.

[21]  M. Robins,et al.  Cerium(IV)-mediated halogenation at C-5 of uracil derivatives , 1990 .

[22]  L. Wiebe,et al.  Synthesis and tumor uptake of 5-bromine-82- and 5-iodine-131-labeled 5-halo-1-(2-fluoro-2-deoxy-.beta.-D-ribofuranosyl)uracils , 1989 .

[23]  L. Townsend Chemistry of Nucleosides and Nucleotides , 1988, Springer US.

[24]  A. Sartorelli,et al.  Purine and 8-substituted purine arabinofuranosyl and ribofuranosyl nucleoside derivatives as potential inducers of the differentiation of the Friend erythroleukemia. , 1985, Journal of medicinal chemistry.

[25]  A. Sartorelli,et al.  8-Substituted guanosine and 2'-deoxyguanosine derivatives as potential inducers of the differentiation of Friend erythroleukemia cells. , 1985, Journal of medicinal chemistry.

[26]  P. Barr,et al.  NUCLEIC ACID RELATED COMPOUNDS. 39. EFFICIENT CONVERSION OF 5-IODO TO 5-ALKYNYL AND DERIVED 5-SUBSTITUTED URACIL BASES AND NUCLEOSIDES , 1983 .

[27]  E. De Clercq,et al.  Nucleic acid related compounds. 40. Synthesis and biological activities of 5-alkynyluracil nucleosides. , 1983, Journal of medicinal chemistry.

[28]  M. Maccoss,et al.  New procedure for the chlorination of pyrimidine and purine nucleosides , 1981 .

[29]  R. E. Holmes,et al.  Purine Nucleosides. VII. Direct Bromination of Adenosine, Deoxyadenosine, Guanosine, and Related Purine Nucleosides , 1964 .

[30]  R. Beltz,et al.  Growth Inhibition of Escherichia coli by New Thymidine Analogs , 1955 .