Transition-metal-catalyzed formation of trans alkenes via coupling of aldehydes
Zhu SF(祝诗发) ; Liao YX(廖远熹) ; Zhu SZ(朱仕正)
刊名Org. Lett.
2004
卷号6期号:3页码:377-380
ISSN号1523-7060
其他题名过渡金属催化醛的偶联形成完全反式烯烃
通讯作者朱仕正
英文摘要Rh-2(OAC)(4) catalyzed the formation of exclusively trans fluorinated alkenes from aldehydes and pentafluorobenzaldehyde tosylhydrazone salts, which were readily prepared from pentafluorobenzaldehyde using the Bamford-Stevens reaction. A series of pentafluorophenyl-containing alkenes were synthesized from aldehydes in moderate to good yields under mild reaction conditions in a one-pot reaction. It is the first report of coupling two different aldehydes to form exclusively trans alkenes.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ol036197s
语种英语
WOS记录号WOS:000188596200018
公开日期2013-01-18
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/14328]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
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GB/T 7714
Zhu SF,Liao YX,Zhu SZ. Transition-metal-catalyzed formation of trans alkenes via coupling of aldehydes[J]. Org. Lett.,2004,6(3):377-380.
APA 祝诗发,廖远熹,&朱仕正.(2004).Transition-metal-catalyzed formation of trans alkenes via coupling of aldehydes.Org. Lett.,6(3),377-380.
MLA 祝诗发,et al."Transition-metal-catalyzed formation of trans alkenes via coupling of aldehydes".Org. Lett. 6.3(2004):377-380.
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