Synthèse (Testers adénosine-5 -phosphoriques d'amino-alcools, comme inhibiteurs potentiels de l'activation des acides aminés
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/hlca.660490114/fullpdf
Reference10 articles.
1. J.-P. Waller, T. Erdös, Doris Leblond, Françoise Lemoine, Ed. Sandrin & R. A. Boissonnas, Biochim. biophysica Acta, sous presse.
2. Studies on Polynucleotides. XVI.1 Specific Synthesis of the C3″-C5″ Interribonucleotidic Linkage. Examination of Routes Involving Protected Ribonucleosides and Ribonucleoside-3″ Phosphates. Syntheses of Uridylyl-(3″→5″)-adenosine, Uridylyl-(3″→5″)-cytidine, Adenylyl-(3″→5″)-adenosine and Related Compounds2
3. Studies on Polynucleotides. I. A New and General Method for the Chemical Synthesis of the C5″-C3″ Internucleotidic Linkage. Syntheses of Deoxyribo-dinucleotides1
4. Studies on Polynucleotides. XXVIII.1 The Specific Synthesis of C3″-C5″-Linked Ribooligonucleotides (4).2 The Stepwise Synthesis of Uridylyl-(3″ → 5″)-adenylyl-(3″ → 5″)-uridylyl-(3″ → 5″)-uridine3
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1. Synthesis of 8-aminoadenosine 5′-(aminoalkyl phosphates), analogues of aminoacyl adenylates;Bioorganic & Medicinal Chemistry;2006-04
2. Synthesis of Peptidinol Adenylates;Nucleosides and Nucleotides;1998-12
3. One-step transformation of α-amino acids to α-amino aldehydes effected by electrochemical oxidation of Ph3P;Tetrahedron Letters;1992-03
4. A Safe, Simple, One-Pot Preparation of N-Derivatized β-Amino Alcohols and Oxazolidinones from Amino Acids;Synthetic Communications;1991-01
5. A specific inhibitor of the ubiquitin activating enzyme: synthesis and characterization of adenosyl-phospho-ubiquitinol, a nonhydrolyzable ubiquitin adenylate analog;Biochemistry;1990-08-14
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