Thiophenderivate als vielseitige Vorstufen für die Synthese von (Hetero)aromaten und Naturstoffen
Verborgen, aber leistungsstark: Thiophene und ihre gesättigten Analoga haben sich als vielseitige C4‐Bausteine erwiesen, die sich effektiv in der Naturstoffsynthese sowie beim Aufbau funktionalisierter (Hetero)aromaten einsetzen lassen. Dieser Minireview soll einen Überblick über Strategien zur Anwendung dieser schwefelhaltigen heterozyklischen ...
Anna Keimer, Franz‐Lucas Haut
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Synthesis of Tricyclic and Tetracyclic Lactone Derivatives of Thieno[2,3-<i>b</i>]pyrazine or Thieno[2,3-<i>b</i>]quinoline: Preliminary Antitumor and Antiparasitic Activity Evaluation. [PDF]
Martins MF +6 more
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Decoding Guaianolide Biosynthesis: Synthetic Insights into Pseudoguaianolides and Seco-Guaianolides. [PDF]
Kourgiantaki M, Zografos AL.
europepmc +1 more source
Amines tuned controllable carbonylation for the synthesis of γ-lactones and 1,4-diones. [PDF]
Wang Y +6 more
europepmc +1 more source
When Bigger is Better: Lanthanum Complexes of Bis(phenoxy-amidine) FAlen Ligands as Unique Catalysts for the Isoselective Ring-Opening Polymerization of Racemic β-Lactones. [PDF]
Bui TT +7 more
europepmc +1 more source
Phytochemical Profile and Analgesic Properties of Chicory Root Extract in the Hot-Plate Test in Mice. [PDF]
Duda Ł +8 more
europepmc +1 more source
Oleanolic Acid Lactones as Effective Agents in the Combat with Cancers-Cytotoxic and Antioxidant Activity, SAR Analysis, Molecular Docking and ADMETox Profile. [PDF]
Bednarczyk-Cwynar B +4 more
europepmc +1 more source
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CONVERSION OF LACTONE INTO LACTONE HEMITHIOACETAL AND SYNTHESIS OF ENOL LACTONE
Chemistry Letters, 1981Abstract Lactone hemithioacetal was synthesized in good yield from ω-phenylthiocarboxylic acid derived from lactone, and it was converted into enol lactone via the corresponding sulfoxide.
Masahito Ochiai +3 more
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Preparation of some simple lactone analogues of picrotoxin and their biological evaluation is reported. Certain analogues possessed activity, but at potencies insufficient to warrant further work.
J D, McChesney, A F, Wycpalek
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