Organocatalytic Asymmetric Fluorination/Semipinacol Rearrangement: An Efficient Approach to Chiral beta-Fluoroketones

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	Organocatalytic Asymmetric Fluorination/Semipinacol Rearrangement: An Efficient Approach to Chiral beta-Fluoroketones
刊名	CHEMISTRY-A EUROPEAN JOURNAL
	2012-10
卷号	18 期号:41
关键词	asymmetric catalysis cinchona alkaloids fluorination organocatalysis rearrangement
ISSN号	0947-6539
通讯作者	Tu, YQ (reprint author), Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China.
学科主题	Chemistry
资助信息	NSFC [21072085, 20921120404, 21102061, 20972059]; National Basic Research Program of China ("973" Program) [2010CB833203]; "111" Program of MOE; National S&T Major Project of China [2012ZX09201101-003]; [86007]
语种	英语
WOS记录号	WOS:000309239300005
内容类型	期刊论文
源URL	[http://202.201.7.4:8080/handle/262010/75598]
专题	化学化工学院_期刊论文
推荐引用方式 GB/T 7714	. Organocatalytic Asymmetric Fluorination/Semipinacol Rearrangement: An Efficient Approach to Chiral beta-Fluoroketones[J]. CHEMISTRY-A EUROPEAN JOURNAL,2012,18(41).
APA	(2012).Organocatalytic Asymmetric Fluorination/Semipinacol Rearrangement: An Efficient Approach to Chiral beta-Fluoroketones.CHEMISTRY-A EUROPEAN JOURNAL,18(41).
MLA	"Organocatalytic Asymmetric Fluorination/Semipinacol Rearrangement: An Efficient Approach to Chiral beta-Fluoroketones".CHEMISTRY-A EUROPEAN JOURNAL 18.41(2012).