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Title: A diastereoselective one-pot, three-step cascade toward α-substituted allylboronic esters. Author: Böse D, Niesobski P, Lübcke M, Pietruszka J. Journal: J Org Chem; 2014 May 16; 79(10):4699-703. PubMed ID: 24745807. Abstract: A new highly diastereoselective synthesis of chiral α-substituted allylboronic esters, based on a one-pot, three-step cascade, is presented. The palladium- and acid-cocatalyzed reaction cascade involves a desilylation of a TBS-protected allylic alcohol, borylation, and addition of an allyl group to an aldehyde. Herein we present the first application of a TBS-protected allylic alcohol in a palladium-catalyzed borylation/allylation reaction.[Abstract] [Full Text] [Related] [New Search]