Pyridine-catalyzed desulfonative borylation of benzyl sulfones

Herein, we report the transition-metal free, pyridine-catalyzed desulfonative borylation of benzyl sulfones with bis(pinacolato)diboron (B 2 pin 2 ). A variety of benzhydryl- and benzyl boronic esters could be synthesized from readily prepared sulfone derivatives. The borylation of cyclic sulfones a...

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Veröffentlicht in:Organic & biomolecular chemistry 2019-08, Vol.17 (31), p.73-733
Hauptverfasser: Maekawa, Yuuki, Ariki, Zachary T, Nambo, Masakazu, Crudden, Cathleen M
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Sprache:eng
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Zusammenfassung:Herein, we report the transition-metal free, pyridine-catalyzed desulfonative borylation of benzyl sulfones with bis(pinacolato)diboron (B 2 pin 2 ). A variety of benzhydryl- and benzyl boronic esters could be synthesized from readily prepared sulfone derivatives. The borylation of cyclic sulfones accompanied by ring opening also proceeded to afford the corresponding sulfonate, which could be converted into functionalized sulfones and sulfonamides. Herein, we report the transition-metal free, pyridine-catalyzed desulfonative borylation of benzyl sulfones with bis(pinacolato)diboron (B 2 pin 2 ).
ISSN:1477-0520
1477-0539
DOI:10.1039/c9ob01099h