首页> 外文期刊>The Journal of Organic Chemistry >Metal-Catalyzed Cycloisomerization Reactions of cis-4-Hydroxy-5-alkynylpyrrolidinones and cis-5-Hydroxy-6-alkynylpiperidinones:Synthesis of Furo[3,2-b]pyrroles and Furo[3,2-b]pyridines
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Metal-Catalyzed Cycloisomerization Reactions of cis-4-Hydroxy-5-alkynylpyrrolidinones and cis-5-Hydroxy-6-alkynylpiperidinones:Synthesis of Furo[3,2-b]pyrroles and Furo[3,2-b]pyridines

机译:顺式-4-羟基-5-炔基吡咯烷酮和顺式-5-羟基-6-炔基哌啶子酮的金属催化环化反应:呋喃[3,2-b]吡咯和呋喃[3,2-b]吡啶的合成

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摘要

Furo[3,2-b]pyrroles and furo[3,2-b]pyridines can be conveniently prepared in good yields from thecycloisomerization reactions of cis-4-hydroxy-5-alkynylpyrrolidinones and cis-5-hydroxy-6-alky-nylpiperidinones, respectively, using Ag(I), Pd(II)/Cu(I), or Au(I) catalysis. In one case, thecycloisomerization product was unstable and produced a furan derivative by a ring-opening reaction.
机译:呋喃并[3,2-b]吡咯和呋喃并[3,2-b]吡啶可以方便地由顺-4-羟基-5-炔基吡咯烷酮与顺-5-羟基-6-烷基-的环异构化反应制得分别使用Ag(I),Pd(II)/ Cu(I)或Au(I)催化的乙烯基哌啶酮。在一种情况下,环异构化产物不稳定并且通过开环反应产生呋喃衍生物。

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