Synthesis of γ-lactones by desymmetrization. A synthesis of (−)-muricatacin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference35 articles.
1. Muricatacin: A simple biologically active acetogenin derivative from the seeds of annona muricata (annonaceae)
2. A general approach to γ-lactones via osmium-catalyzed asymmetric dihydroxylation. Synthesis of (−)- and (+)-muricatacin.
3. Stereoselective Synthesis of the Cytotoxic Acetogenins (+)- and (-)-Muricatacin
4. Tetrahydrofurane und γ-Lactone, V[1,2] Optisch aktive δ-Hydroxy-γ-lactone aus Cyclooctin und Furan — Synthese von (—)-(R,R)- und (+)-(S,S)-Muricatacin sowie verwandter Verbindungen
5. Enantioselective Synthesis of (+)- and (-)-Muricatacin through SE2' Addition of Nonracemic .gamma.-Silyloxy Allylic Stannanes to Aldehydes
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1. A Historical Review of the Total Synthesis of Natural Products Developed in Portugal;European Journal of Organic Chemistry;2023-03-25
2. Divergent synthesis and antitumour activity of novel conformationally constrained (−)-muricatacin analogues;Journal of the Serbian Chemical Society;2023
3. First total synthesis of 7-thia-(-)-muricatacin;Results in Chemistry;2022-01
4. Synthesis of disubstituted γ-butyrolactones and spirocyclopropanes via a multicomponent reaction of aldehydes, Meldrum's acid and sulfoxonium ylides;Organic Chemistry Frontiers;2021
5. Stereoselective Sequential Spirocyclopropanation/Cloke–Wilson Rearrangement Reactions for Synthesis of trans-β,γ-Disubstituted γ-Butyrolactones Using Alkylidene Meldrum’s Acid and Benzyl Halides;The Journal of Organic Chemistry;2020-01-10
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