Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement

標題:	Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement
作者:	Wu, HJ Tsai, SH Chung, WS 應用化學系 Department of Applied Chemistry
公開日期:	4-十一月-1996
摘要:	Treatment of the endo-thioester group substituted norbornenes 3a-3d with iodine in aqueous tetrahydrofuran at 25 degrees C gave the novel methylthio group rearranged lactonization products 4a-4d in 80% yields; iodolactonization reaction of 9 was applied to the synthesis of novel diacetal trioxa-cage compound 13. Copyright (C) 1996 Elsevier Science Ltd
URI:	http://dx.doi.org/10.1016/0040-4039(96)01869-2 http://hdl.handle.net/11536/933
ISSN:	0040-4039
DOI:	10.1016/0040-4039(96)01869-2
期刊:	TETRAHEDRON LETTERS
Volume:	37
Issue:	45
起始頁:	8209
結束頁:	8212
顯示於類別：	期刊論文

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