An Expedient Synthesis of Oxindole Dimers by Direct Oxidative Dimerization of Oxindoles 


Vol. 34,  No. 8, pp. 2446-2450, Aug.  2013
10.5012/bkcs.2013.34.8.2446


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  Abstract

Oxindole dimers have been used as intermediates in the synthesis of various cyclotryptamine alkaloids. An efficient direct synthesis of oxindole dimers has been carried out from 3-substituted oxindoles via an oxidative dimerization using manganese(III) acetate or copper acetate/silver acetate system.

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[IEEE Style]

H. J. Lee, S. Lee, J. W. Lim, J. N. Kim, "An Expedient Synthesis of Oxindole Dimers by Direct Oxidative Dimerization of Oxindoles," Bulletin of the Korean Chemical Society, vol. 34, no. 8, pp. 2446-2450, 2013. DOI: 10.5012/bkcs.2013.34.8.2446.

[ACM Style]

Hyun Ju Lee, Sangku Lee, Jin Woo Lim, and Jae Nyoung Kim. 2013. An Expedient Synthesis of Oxindole Dimers by Direct Oxidative Dimerization of Oxindoles. Bulletin of the Korean Chemical Society, 34, 8, (2013), 2446-2450. DOI: 10.5012/bkcs.2013.34.8.2446.

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ISSN(Print) 0253-2964
ISSN(Online) 1229-5949