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dc.contributor.authorWu, HJen_US
dc.contributor.authorYen, CHen_US
dc.contributor.authorChuang, CTen_US
dc.date.accessioned2019-04-02T05:58:27Z-
dc.date.available2019-04-02T05:58:27Z-
dc.date.issued1996-10-07en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/0040-4039(96)01686-3en_US
dc.identifier.urihttp://hdl.handle.net/11536/149327-
dc.description.abstractThe base-catalyzed intramolecular Diels-Alder reactions of 5-trimethylsilyl-2-furfuryl propargyl ethers la-lf gave compounds 2a-2f and 3a-3f in 70-90% yields respectively, a novel reaction involving an intramolecular Diels-Alder reaction followed by a trimethylsilyl group 1,2-rearrangement and Brook rearrangement. Copyright (C) 1996 Elsevier Science Ltden_US
dc.language.isoen_USen_US
dc.titleIntramolecular Diels-Alder reaction of furans with allenyl ethers followed by trimethylsilyl group 1,2-rearrangement and Brook rearrangementen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0040-4039(96)01686-3en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume37en_US
dc.citation.spage7395en_US
dc.citation.epage7398en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1996VL42100019en_US
dc.citation.woscount8en_US
Appears in Collections:Articles


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