Enantio- and Diastereoselective Synthesis of Hydroxy Bis(boronates) via Cu-Catalyzed Tandem Borylation/1,2-Addition

Catalytic enantioselective synthesis of 1-hydroxy-2,3-bisboronate esters through multicomponent borylation/1,2-addition is reported. Catalyst and substrates are readily available, form both a C–B and C–C bond, and generate up to three contiguous stereocenters. The reaction is tolerant of aryl, vinyl...

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Veröffentlicht in:ACS catalysis 2017-07, Vol.7 (7), p.4441-4445
Hauptverfasser: Green, Jacob C, Joannou, Matthew V, Murray, Stephanie A, Zanghi, Joseph M, Meek, Simon J
Format: Artikel
Sprache:eng
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Zusammenfassung:Catalytic enantioselective synthesis of 1-hydroxy-2,3-bisboronate esters through multicomponent borylation/1,2-addition is reported. Catalyst and substrates are readily available, form both a C–B and C–C bond, and generate up to three contiguous stereocenters. The reaction is tolerant of aryl, vinyl, and alkyl aldehydes and ketones in up to 95% yield, >20:1 dr, and 99:1 er. Intramolecular additions to aldehydes and ketones result in stereodivergent processes. The hydroxy bis­(boronate) ester products are amenable to site-selective chemical elaboration.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.7b01123