| 1 |
SNAr displacements with 6-(fluoro, chloro, bromo, iodo, and alkylsulfonyl)purine nucleosides: Synthesis, kinetics, and mechanism
Liu JQ, Robins MJ
Journal of the American Chemical Society, 129(18), 5962, 2007 |
| 2 |
Biomimetic simulation of free radical-initiated cascade reactions postulated to occur at the active site of ribonucleotide reductases
Robins MJ, Guo ZQ, Samano MC, Wnuk SF
Journal of the American Chemical Society, 121(7), 1425, 1999 |
| 3 |
Nucleic acid related compounds. 109. Biomimetic modeling of the first substrate reaction at the active site of ribonucleotide reductases. Abstraction of H3 ' by a thiyl free radical
Robins MJ, Ewing GJ
Journal of the American Chemical Society, 121(24), 5823, 1999 |
| 4 |
Elimination of Chlorine (Radical) or Tosylate (Anion) from C2’ of Nucleoside C3’ Free-Radicals as Model Reactions Postulated to Occur at the Active-Site of Ribonucleotide Reductases
Robins MJ, Guo ZQ, Wnuk SF
Journal of the American Chemical Society, 119(15), 3637, 1997 |
| 5 |
Stannyl Radical-Mediated Cleavage of Pi-Deficient Heterocyclic Sulfones - Synthesis of Alpha-Fluoro Esters and the First Homonucleoside Alpha-Fluoromethylene Phosphonate
Wnuk SF, Robins MJ
Journal of the American Chemical Society, 118(10), 2519, 1996 |
| 6 |
Biomimetic Modeling of the Decomposition of 2’-Chloro-2’-Deoxynucleotides by Ribonucleotide Reductases to Give 3(2H)-Furanones Which Can Effect Mechanism-Based Inactivation by Michael-Type Alkylation
Robins MJ, Guo ZQ, Samano MC, Wnuk SF
Journal of the American Chemical Society, 118(45), 11317, 1996 |
| 7 |
Nucleic-Acid Related-Compounds .91. Biomimetic Reactions Are in Harmony with Loss of 2’-Substituents as Free-Radicals (Not Anions) During Mechanism-Based Inactivation of Ribonucleotide Reductases - Differential Interactions of Azide, Halogen, and Alkylthio Groups with Tributylstannane and Triphenylsilane
Robins MJ, Wnuk SF, Hernandezthirring AE, Samano MC
Journal of the American Chemical Society, 118(46), 11341, 1996 |
| 8 |
Nucleic-Acid Related-Compounds .86. Nucleophilic Functionalization of Adenine, Adenosine, Tubercidin, and Formycin Derivatives via Elaboration of the Heterocyclic Amino Group into a Readily Displaced 1,2,4-Triazol-4-Yl Substituent
Miles RW, Samano V, Robins MJ
Journal of the American Chemical Society, 117(22), 5951, 1995 |
| 9 |
Efficient Conversion of 6-Aminopurines and Nucleosides into 6-Substituted Analogs via Novel 6-(1,2,4-Triazol-4-Yl)Purine Derivatives
Samano V, Miles RW, Robins MJ
Journal of the American Chemical Society, 116(20), 9331, 1994 |
