期刊
TETRAHEDRON LETTERS
卷 54, 期 21, 页码 2685-2689出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2013.03.070
关键词
Knoevenagel-hetero-Diels-Alder; Domino reaction; Indoline-2-thiones; Aqueous medium; Benzo-delta-sultones; Thiopyrano indole
An efficient synthesis of novel pentacyclic thiopyrano indole-annulated benzo-delta-sultone derivatives is achieved via intramolecular domino Knoevenagel-hetero-Diels-Alder reaction of 2-formylphenyl (E)-2-phenylethenyl sulfonates and indoline-2-thiones in aqueous medium. The products are formed in good yields with high regio- and stereoselectivity. (c) 2013 Elsevier Ltd. All rights reserved.
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