Petasis three-component reactions for the synthesis of diverse heterocyclic scaffolds
1Department of Chemistry, Technical University of Denmark, Kongens Lyngby DK-2800, Denmark; Department of Immunology and Microbiology, University of Copenhagen, Copenhagen DK-2200, Denmark; Chemical Biology and Therapeutics Science, Broad Institute of MIT and Harvard, Cambridge, MA 02142, United States; Department of Medicine, Harvard Medical School, Boston, MA 02115, United States; Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, United States; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, United States.
Abstract:
The Petasis three-component reaction (PR) of hydroxy aldehydes, amines and boronic acids is an important multi-component reaction for the synthesis of structurally diverse scaffolds and biologically interesting small molecules. The reaction has been significantly explored in the past decade, and many new variants have emerged, such as asymmetric, traceless and four-component approaches. The excellent stereoselectivity, high yield and broad functional group tolerance altogether make this reaction ideal for fragment and compound collection synthesis, since orthogonal chemical handles can be incorporated for subsequent scaffold formation and appendage modification. Herein we present a selection of recent variations on the PR theme for the synthesis of scaffolds of relevance to medicinal chemistry.
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