Enantioselective synthesis of (+)-patulolide C via proline-catalyzed sequential α-aminooxylation and Horner–Wadsworth–Emmons olefination
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Structure of patulolide a, a new macrolide from mutants
2. New macrolides from Penicillium urticae mutant S11R59.
3. 1,8-Stereocontrol by 1,5-induction using an allylstannane followed by Ireland-Claisen rearrangement: Diastereoselective total synthesis of (±)-patulolide C
4. The Synthesis of (±)-Patulolide C and its Epimer Via Dodec-3-En-11-Olide
5. Asymmetric Synthesis of the Seco-Acids of (R,R)-Pyrenophorin and (R)-Patulolide A Monitored by a Chiral Sulfoxide Group
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1. Synthesis of enantioenriched α-heteroatom functionalised aldehydes by chiral organocatalysis and their synthetic applications;Organic Chemistry Frontiers;2021
2. Organocatalyzed α-aminooxylation/amination of aldehydes and their sequential reactions: A versatile tool for the synthesis of bioactive molecules;Bioactive Natural Products;2020
3. Enantioselective Cobalt‐Catalysed Transformations;Cobalt Catalysis in Organic Synthesis;2019-12-20
4. Asymmetric Synthesis of Saturated Hydroxy Fatty Acids and Fatty Acid Esters of Hydroxy Fatty Acids;European Journal of Organic Chemistry;2019-02-25
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