A borane-mediated palladium-catalyzed reductive allylic alkylation of α,β-unsaturated carbonyl compounds
Author:
Affiliation:
1. Departmentof Chemistry
2. Stanford University
3. Stanford
4. USA
Abstract
A palladium-catalyzed allylation of ester-derived boron enolates, which is prepared through 1,4-reduction of α,β-unsaturated ester analogues.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/SC/C9SC05970A
Reference51 articles.
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3. Enolboration. 2. Dicyclohexylchloroborane/triethylamine as a convenient reagent for regio- and stereoselective enolboration of representative classes of ketones
4. A new approach to (Z)-vinyloxyboranes via 1,4 hydroboration of (E)-α,β-unsaturated ketones. Synthesis of syn aldols
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