Synthesis of novel silylated 1,2,4-triazin-5-ones

[1]  B. Stoltz,et al.  Synthesis of bis(indole)-1,2,4-triazinones , 2005 .

[2]  C. Bolm,et al.  Enantiopure α-Silyl-Substituted α-Hydroxyacetic Acids Using O-H Insertion Methodology and Boron-Based Asymmetric Reductions , 2005 .

[3]  S. Sieburth,et al.  α-Trialkylsilyl Amino Acid Stability , 2005 .

[4]  C. Bolm,et al.  Intermolecular rhodium(II)-catalyzed reactions with silicon-substituted carbonyl ylides. , 2002, Organic letters.

[5]  A. S. Shawali,et al.  Regioselectivity in 1,5-electrocyclization of N-[as-triazin-3-yl]nitrilimines. Synthesis of s-triazolo[4,3-b]-as-triazin-7(8H)-ones , 2002 .

[6]  K. Drauz,et al.  Synthesis and use of alpha-silyl-substituted alpha-hydroxyacetic acids. , 2002, Organic letters.

[7]  E. Banfi,et al.  Synthesis and antimycobacterial activity of some 4H-1,2,4-triazin-5-one derivatives. , 2000, Farmaco.

[8]  R. Tacke,et al.  Syntheses and Properties of Silicon- and Germanium-Containing α-Amino Acids and Peptides: A Study on C/Si/Ge Bioisosterism§ , 2000 .

[9]  K. Drauz,et al.  α-Trialkylsilyl-Substitutedα-Amino Acids , 2000 .

[10]  K. Lemr,et al.  Synthesis of some polycyclic 1,2,4-triazines disposing of acidic N-H group , 2000 .

[11]  C. Ehrhardt,et al.  Design, synthesis and biological evaluation of selective boron-containing thrombin inhibitors. , 1999, Bioorganic & medicinal chemistry.

[12]  Z. G. Aliev,et al.  Reactions of aroylpyruvic acids withS-methylisothiosemicarbazide hydroiodide and studies of the crystal structures of the reaction products , 1998 .

[13]  M. Mafi,et al.  Regioselective N-Methylation of Methylthio-Substituted Pyrimidinones and 1,2,4-Triazinone with Methanol over H-Y Zeolite. , 1997 .

[14]  B. Weidmann.  (Trimethylsilyl)alanine: a Metabolically Stable 'Bio-Isostere' for Phenylalanine , 1992, CHIMIA.

[15]  E. El‐Ashry,et al.  Synthesis of γ-butyrolactones, quinoxalines, and azauracils from 4-aryl-2-oxobutanoic acid derivatives , 1988 .

[16]  E. Taylor,et al.  Intramolecular Diels-Alder reactions of 1,2,4-triazines. Synthesis of condensed pyrimidines , 1987 .

[17]  Jim J. Huang.  Synthesis of fused 1,2,4-triazines: 6- and 7-azapteridine and 6-azapurine ring systems , 1985 .

[18]  Z. Yoshida,et al.  Palladium-catalyzed polyhetero-Claisen rearrangement of 3-(allylthio)-1,2,4-triazin-5(4H)-ones , 1983 .

[19]  F. Westheimer,et al.  The purification of orotidine-5'-phosphate decarboxylase from yeast by affinity chromatography. , 1979, The Journal of biological chemistry.

[20]  G. Just,et al.  C-Nucleosides and related compounds. XII. The synthesis of the carbocyclic analogues of D, L-6-azapseudouridine, 2-thio-6-azapseu douridine, and pyrazofurin A. On the cyclization of semicarbazones of α-keto esters , 1977 .

[21]  M. Joullié,et al.  3,5-Disubstituted 6-benzyl-1,2,4-triazines: syntheses and reactions , 1976 .

[22]  A. Trebst,et al.  [Structure-activity correlation with respect to 1,2,4-triazinones, a new group of photosynthesis inhibitors (1)]. , 1968, Die Naturwissenschaften.

[23]  S. Watanabe,et al.  SYNTHESES AND ANTIVIRAL ACTIVITY OF 3-THIOXO-6-ARYL-3,4-DIHYDRO-AS-TRIAZIN-5(2H)-ONE AND 6-ARYL-AS-TRIAZINE-3,5(2H,4H)-DIONE. , 1963, Chemical & pharmaceutical bulletin.