ChemInform Abstract: Superacid-Promoted Dual C-C Bond Formation by Friedel-Crafts Alkylation/Acylation of Cinnamate Esters: Synthesis of Indanones

In the case of cinnamic esters (I), the indanone is formed by cyclization of the more electron‐rich aryl moiety: arene reactant for (III), (V), (VII)/(VIII) and (IX) or cinnamic ester for (X) and (XII).

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Veröffentlicht in:ChemInform 2015-09, Vol.46 (39), p.no-no
Hauptverfasser: Ramulu, Bokka Venkat, Niharika, Pedireddi, Satyanarayana, Gedu
Format: Artikel
Sprache:eng
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Zusammenfassung:In the case of cinnamic esters (I), the indanone is formed by cyclization of the more electron‐rich aryl moiety: arene reactant for (III), (V), (VII)/(VIII) and (IX) or cinnamic ester for (X) and (XII).
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201539084