Allylation of aldehydes via Umpolung of π-allylpalladium(II) with triethylborane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Novel carbonyl-dependent regioselective allylation via diethylzinc-mediated umpolung of π-allylpalladium
2. Unique regio- and stereoselectivity in the allylation of benzaldehyde with 2-substituted allylzincs generated by umpolung of π-allylpalladium
3. Propargylation of Carbonyl Compounds by Umpolung of Propargylpalladium Complexes with Diethylzinc
4. Highly Stereoselective Allylation of Benzaldehyde: Generation of a Stereochemically Defined Allylzinc Species from aπ-Allylpalladium Intermediate and Diethylzinc
5. Novel catalytic reactions involving π-allylpalladium and -nickel as the key intermediates: umpolung and β-decarbopalladation of π-allylpalladium and nickel-catalyzed homoallylation of carbonyl compounds with 1,3-dienes
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2. Copper-Catalyzed Umpolung Reactivity of Propargylic Carbonates in the Presence of Diboronates: One Stone Four Birds;Journal of the American Chemical Society;2023-11-29
3. Catalytic Umpolung Carboxylation of π-Allylpalladium Species with Carbon Dioxide;Journal of Synthetic Organic Chemistry, Japan;2022-09-01
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5. Acyclic Remote 1,5- and 1,4,5-Stereocontrol in the Catalytic Stereoselective Reactions of β-Lactams with Aldehydes: The Effect of the N-Methylimidazole Ligand;The Journal of Organic Chemistry;2018-11-09
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