4.3 Article

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

Journal

BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume 34, Issue 8, Pages 2446-2450

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.5012/bkcs.2013.34.8.2446

Keywords

Oxindole dimers; Oxidative dimerization; Manganese(BI) acetate; Oxindoles

Funding

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology [2012R1A1B3000541]
  3. National Research Foundation of Korea [2012R1A1B3000541] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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(BI) acetate or copper acetate/silver acetate system.

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