Int. J. Mol. Sci. 2003, 4(6), 371-378; doi:10.3390/i4060371
Article

C- versus O-Arylation of an Enol-Lactone Using Potassium tert-butoxide

1,2,* email, 1 and 2
Received: 31 October 2002; Accepted: 6 March 2003 / Published: 31 May 2003
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: The use of potassium tert-butoxide as the base in arylation reactions of an enollactone with a series of benzyl halides was explored. Our work demonstrates that the ratio of C-arylation to O-arylation varies with the substitution pattern of the aryl halide.
Keywords: Arylation; Enol-lactone; Potassium tert-butoxide
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MDPI and ACS Style

Ibrahimi, S.; Sauvé, G.; Essassi, E.M. C- versus O-Arylation of an Enol-Lactone Using Potassium tert-butoxide. Int. J. Mol. Sci. 2003, 4, 371-378.

AMA Style

Ibrahimi S, Sauvé G, Essassi EM. C- versus O-Arylation of an Enol-Lactone Using Potassium tert-butoxide. International Journal of Molecular Sciences. 2003; 4(6):371-378.

Chicago/Turabian Style

Ibrahimi, Sanae; Sauvé, Gilles; Essassi, El M. 2003. "C- versus O-Arylation of an Enol-Lactone Using Potassium tert-butoxide." Int. J. Mol. Sci. 4, no. 6: 371-378.

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