Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence

Young Keun Yang, Jung Hoon Choi, Jinsung Tae

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An efficient method for the synthesis of 2,3- and 2,3,4-substituted furans starting from acyclic enynes was developed using an enyne-RCM/Diels-Alder reaction sequence. The reaction conditions for the transformation of 1,2-dioxines having an adjacent 1,2-oxazine ring into furans and the cleavage of N-O bonds are discussed.

Original languageEnglish
Pages (from-to)6995-6998
Number of pages4
JournalJournal of Organic Chemistry
Issue number17
Publication statusPublished - 2005 Aug 19


All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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