Intramolecular Diels-Alder reaction of furans with allenyl ethers followed by trimethylsilyl group 1,2-rearrangement and Brook rearrangement

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Wu, HJ	en_US
dc.contributor.author	Yen, CH	en_US
dc.contributor.author	Chuang, CT	en_US
dc.date.accessioned	2019-04-02T05:58:27Z	-
dc.date.available	2019-04-02T05:58:27Z	-
dc.date.issued	1996-10-07	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/0040-4039(96)01686-3	en_US
dc.identifier.uri	http://hdl.handle.net/11536/149327	-
dc.description.abstract	The 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 Ltd	en_US
dc.language.iso	en_US	en_US
dc.title	Intramolecular Diels-Alder reaction of furans with allenyl ethers followed by trimethylsilyl group 1,2-rearrangement and Brook rearrangement	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/0040-4039(96)01686-3	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	37	en_US
dc.citation.spage	7395	en_US
dc.citation.epage	7398	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:A1996VL42100019	en_US
dc.citation.woscount	8	en_US
顯示於類別：	期刊論文