Nickel-Catalyzed Diastereoselective Cross-Electrophile Ring Opening of 7-Oxabenzonorbornadienes with Aromatic Aldehydes.
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DOI: 10.1021/acs.orglett.3c00471
Abstract: In this protocol, we developed a nickel-catalyzed diastereoselective cross-electrophile ring opening reaction of 7-oxabenzonorbornadienes with aromatic aldehydes as the electrophilic coupling partner utilizing Zn as the stoichiometric reductant. In this reaction, a challenging stereoselective bond… read more here.
Keywords: electrophile ring; nickel catalyzed; catalyzed diastereoselective; diastereoselective cross ... See more keywords