Stereoselective Direct Amine-Catalyzed Decarboxylative Aldol Addition
Author:
Affiliation:
1. Department of Chemistry, Humboldt-University, Brook-Taylor Str. 2, 12 489 Berlin, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol200412r
Reference28 articles.
1. REGIOSPECIFIC ALDOL SYNTHESIS. THE GENERATION OF ACTIVE ENOLATES BY THE REDUCTION OF 2,2,2-TRICHLOROETHYL ESTERS OF α-SUBSTITUTED-β-KETO ACIDS WITH Zn
2. The palladium-catalyzed directed aldol reaction of aldehydes with ketone enolates generated by the decarboxylation of allyl .beta.-keto carboxylates under neutral conditions
3. NiCl2(PPh3)2–Zn Promoted Deallyloxycarbonylative Directed Aldo Reaction of Allyl β-Keto Carboxylates with Aldehydes to β-Hydroxy Ketones
4. A Tandem Claisen-Decarboxylation-Aldol Reaction – Facile Access to The Fredericamycin A Core
5. Decarboxylative Aldol Reactions of Allyl β-Keto Esters via Heterobimetallic Catalysis
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