Synthesis of gem-difluoromethylenated analogues of boronolide

	Synthesis of gem-difluoromethylenated analogues of boronolide
	Lin J(林静) ; Qiu XL(邱小龙) ; Qing FL(卿凤翎)
刊名	Beilstein J. Org. Chem.
	2010
卷号	6 页码:37
ISSN号	1860-5397
其他题名	Synthesis of gem-difluoromethylenated analogues of boronolide
通讯作者	卿凤翎
英文摘要	The straightforward synthesis of four gem-difluoromethylenated analogues 4-7 of boronolide is described. The key steps of the synthesis include the concise preparation of the key intermediates 12a-b through the indium-mediated gem-difluoropropargylation of aldehyde 9 with the fluorine-containing building block 11 and the efficient construction of alpha,beta-unsaturated-delta-lactones 15a-b via BAIB/TEMPO-procedure.
学科主题	氟化学
收录类别	SCI
原文出处	http://dx.doi.org/10.3762/bjoc.6.37
语种	英语
WOS记录号	WOS:000277432500001
公开日期	2013-02-22
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/17679]
专题	上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式 GB/T 7714	Lin J,Qiu XL,Qing FL. Synthesis of gem-difluoromethylenated analogues of boronolide[J]. Beilstein J. Org. Chem.,2010,6:37.
APA	林静,邱小龙,&卿凤翎.(2010).Synthesis of gem-difluoromethylenated analogues of boronolide.Beilstein J. Org. Chem.,6,37.
MLA	林静,et al."Synthesis of gem-difluoromethylenated analogues of boronolide".Beilstein J. Org. Chem. 6(2010):37.