Decoding Products of Diversity Pathways from Stock Solutions Derived from Single Polymeric Macrobeads
- 14 September 2001
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 40 (18) , 3421-3425
- https://doi.org/10.1002/1521-3773(20010917)40:18<3421::aid-anie3421>3.0.co;2-b
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Asymmetric Catalysis in Diversity-Oriented Organic Synthesis: Enantioselective Synthesis of 4320 Encoded and Spatially Segregated DihydropyrancarboxamidesAngewandte Chemie International Edition in English, 2001
- Asymmetric Catalysis in Diversity-Oriented Organic Synthesis: Enantioselective Synthesis of 4320 Encoded and Spatially Segregated DihydropyrancarboxamidesAngewandte Chemie, 2001
- An Alkylsilyl-Tethered, High-Capacity Solid Support Amenable to Diversity-Oriented Synthesis for One-Bead, One-Stock Solution Chemical GeneticsJournal of Combinatorial Chemistry, 2001
- Split−Pool Synthesis of 1,3-Dioxanes Leading to Arrayed Stock Solutions of Single Compounds Sufficient for Multiple Phenotypic and Protein-Binding AssaysJournal of the American Chemical Society, 2001
- Target-Oriented and Diversity-Oriented Organic Synthesis in Drug DiscoveryScience, 2000
- Chemical genetics resulting from a passion for synthetic organic chemistryBioorganic & Medicinal Chemistry, 1998
- Encoding methods for combinatorial chemistry.Current Opinion in Chemical Biology, 1997
- A General Method for Molecular Tagging of Encoded Combinatorial Chemistry LibrariesThe Journal of Organic Chemistry, 1994
- Complex synthetic chemical libraries indexed with molecular tags.Proceedings of the National Academy of Sciences, 1993
- Alkylation of benzene with α-diazoketones via cycloheptatrienyl intermediatesJournal of the Chemical Society, Chemical Communications, 1985