Multiple-Component Condensation Strategies for Combinatorial Library Synthesis
Authors:
- 13 March 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Accounts of Chemical Research
- Vol. 29 (3) , 123-131
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- A solid phase protocol of the biginelli dihydropyrimidine synthesis suitable for combinatorial chemistryTetrahedron Letters, 1995
- DIVERSITY OF OLIGONUCLEOTIDE FUNCTIONSAnnual Review of Biochemistry, 1995
- A review of the utility of soluble peptide combinatorial librariesBiopolymers, 1995
- Applications of Combinatorial Technologies to Drug Discovery. 1. Background and Peptide Combinatorial LibrariesJournal of Medicinal Chemistry, 1994
- The generation of molecular diversityBioorganic & Medicinal Chemistry Letters, 1993
- Rational screening of oligonucleotide combinatorial libraries for drug discoveryNucleic Acids Research, 1993
- A general and expedient method for the solid-phase synthesis of 1,4-benzodiazepine derivativesJournal of the American Chemical Society, 1992
- Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesisJournal of the American Chemical Society, 1992
- Peptoids: a modular approach to drug discovery.Proceedings of the National Academy of Sciences, 1992
- Multiple Peptide Synthesis Methods and Their Applications. New Synthetic Methods (87)Angewandte Chemie International Edition, 1992