4.4 Article

Synthesis of 2,4-disubstituted 3-chlorofurans and the effect of the chlorine substituent in furan Diels-Alder reactions

期刊

TETRAHEDRON LETTERS
卷 49, 期 5, 页码 799-802

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2007.11.193

关键词

3-chlorofurans; 3,3-dichlorotetrahydrofurans; radical cyclization; Diels-Alder reaction; dehydrochlorination; chlorine effect

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2,4-Disubstituted 3-chlorofurans were synthesized in 42-69% overall yields by CuCl/bpy-catalyzed halogen atom transfer radical cyclization of 1-substituted 2,2,2-trichloroethyl allyl ethers to 2-substituted 3,3-dichloro-4-(1-chloroalkyl)tetrahydrofurans followed by base promoted dehydrochlorination. Diets-Alder reactions of 4-substituted 2-(2-furyl)-, 2-styryl-, and 2-crotyl-3-chlorofurans with dimethyl acetylenedicarboxylate occurred exclusively on the chlorofurano diene moieties and not on the non-chlorinated furano diene or the chlorinated exocyclic diene alternatives, demonstrating the predominance of the halogen effect in the furan Diels-Alder reaction. (C) 2007 Elsevier Ltd. All rights reserved.

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