Organolithium mediated synthesis of prenylchalcones as potential inhibitors of chemoresistance

Tetrahedron Letters

Volumn 40, Issue 39, 1999, Pages 7095-7098

  Daskiewicz, Jean B ^a   Comte, Gilles ^a   Barron, Denis ^a   Di Pietro, Attilio ^b   Thomasson, François ^c  

^a UNIVERSITÉ LYON 1   (France)

^b INSTITUT DE BIOLOGIE ET CHIMIE DES PROTÉINES   (France)

^c UNIV GRENOBLE ALPES   (France)

Author keywords

Aldol reaction; Biologically active compounds; Chalcones; Protecting groups

Indexed keywords

CHALCONE DERIVATIVE; GLYCOPROTEIN P; ORGANOLITHIUM COMPOUND; PRENYLCHALCONE; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; CANCER CHEMOTHERAPY; CANCER INHIBITION; CANCER RESISTANCE; CATALYSIS; DRUG SYNTHESIS; MULTIDRUG RESISTANCE; POLYMERIZATION; PRENYLATION; REACTION ANALYSIS; TEMPERATURE;

EID: 0033600699     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01461-6     Document Type: Article

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11. 8. Examples of papers reporting the synthesis of prenylchalcones in presence of ethanolic potassium hydroxide: Sherif, E. A.; Islam, A.; Krishnamurti, M. Indian J. Chem. 1982, 21B, 478. Fujimoto, T.; Nomura, T. Heterocycles 1984, 22, 997. Matsumoto, J.; Fujimoto, T.; Takino, C.; Saitoh, M.; Hano, Y.; Fukai, T.; Nomura, T. Chem. Pharm. Bull. 1985, 33, 3250. Bu, X.; Li, Y. J. Nat. Prod. 1996, 59, 968. Bu, X.; Zhao, L.; Li, Y. Synthesis 1997, 1246. Harwood, L. M.; Loftus, G. C.; Oxford, A.; Thomson, C. Synth. Comm. 1990, 20, 649.
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