Chemical Evolution: A Model System That Selects and Amplifies a Receptor for the Tripeptide (d)Pro(l)Val(d)Val

This publication has 16 references indexed in Scilit:

• Use of Molecular Recognition To Drive Chemical Evolution. 1. Controlling the Composition of an Equilibrating Mixture of Simple Arginine Receptors
  Journal of the American Chemical Society, 1997
• Macrocyclic oligomers of isophthalic acid and trans-1,2-diaminocyclohexane — building blocks for synthetic peptide receptors
  Tetrahedron Letters, 1996
• Macrocyclic triamines as linkers in two-armed receptors for peptides
  Bioorganic & Medicinal Chemistry Letters, 1996
• Discovery of Sequence-Selective Peptide Binding by Synthetic Receptors Using Encoded Combinatorial Libraries
  Accounts of Chemical Research, 1996
• Chance and Necessity in the Selection of Nucleic Acid Catalysts
  Accounts of Chemical Research, 1996
• Sequence-Selective Receptors of Peptides. A Simple Molecular Design for Construction of Large Combinatorial Libraries of Receptors
  The Journal of Organic Chemistry, 1996
• Unnatural Selection in Chemical Systems
  Accounts of Chemical Research, 1995
• Cyclooligomeric Receptors Based on Trimesic Acid and 1,2-Diamines. Minimal Structure for Sequence-Selective Peptide Binding
  The Journal of Organic Chemistry, 1995
• Template-directed synthesis: use of a reversible reaction
  Journal of the American Chemical Society, 1992
• The Total Synthesis of Steroids¹
  Journal of the American Chemical Society, 1952