期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 70, 期 17, 页码 6995-6998出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo050957q
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[GRAPHICS] 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.
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