Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10565476 | Current Opinion in Chemical Biology | 2005 | 11 Pages |
Abstract
The amalgamation of two of combinatorial chemistry's most attractive concepts - natural product libraries and multicomponent reactions (MCRs) - should provide a powerful tactic for generating libraries of bioactive compounds. Yet, despite many recent advances in this area, only a few MCRs can deliver functionalized products whose structures closely resemble that of complex polycyclic natural products. A large proportion of recently developed MCRs are based on [4+2] or [3+2] cycloadditions, and isocyanide-based processes. Because of substrate limitations, however, they are not always ideally suitable for applications in diversity-oriented synthesis of natural product-like compounds. A promising area awaiting further development is the use of transition metal-catalyzed cascade reactions.
Related Topics
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Authors
Agnieszka Ulaczyk-Lesanko, Dennis G Hall,