4.4 Article

An efficient ZnO-catalyzed synthesis of novel indole-annulated thiopyrano-chromene derivatives via Domino Knoevenagel-hetero-Diels-Alder reaction

期刊

TETRAHEDRON LETTERS
卷 50, 期 48, 页码 6723-6727

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.09.106

关键词

Knoevenagel reaction; Hetero-Diels-Alder reaction; Indolin-2-thione; O-propargylated salicylaldehyde; ZnO

资金

  1. Islamic Development Bank (IDB)

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An efficient synthesis of pentacyclic indole derivatives is achieved via domino Knoevenagel-hetero-Diels-Alder reactions of indolin-2-thiones and O-propargylated salicylaldehyde derivatives in CH3CN in the presence of 10 mol % of ZnO as a heterogeneous catalyst. The products are formed in good to excellent yields. (C) 2009 Elsevier Ltd. All rights reserved.

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