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dc.contributor.authorQin, Dan-Dan
dc.contributor.authorLai, Wen-Han
dc.contributor.authorHu, Di
dc.contributor.authorChen, Zheng
dc.contributor.authorWu, An-An
dc.contributor.authorRuan, Yuan-Ping
dc.contributor.authorZhou, Zhao-Hui
dc.contributor.authorChen, Hong-Bin
dc.contributor.author陈洪斌
dc.date.accessioned2013-02-28T08:09:00Z
dc.date.available2013-02-28T08:09:00Z
dc.date.issued2012-08
dc.identifier.citationCHEMISTRY-A EUROPEAN JOURNAL,2012,18(34):10515-10518zh_CN
dc.identifier.issn0947-6539
dc.identifier.urihttp://dx.doi.org/10.1002/chem.201201565
dc.identifier.uriWOS:000307387300009
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/15003
dc.description.abstractAmino alcohol–CuII catalyst: Highly enantioselective Henry reactions between aromatic aldehydes and nitromethane have been developed. The reactions were catalyzed by an easily available and operationally simple amino alcohol–copper(II) catalyst (see scheme). In total, 38 substrates were tested and the R-configured products were obtained in good yields with excellent enantioselectivities.zh_CN
dc.description.sponsorshipFundamental Research Funds for the Central Universities [2010121014]; National Natural Science Foundation of China [21133004]zh_CN
dc.language.isoenzh_CN
dc.publisherWILEY-V C H VERLAG GMBHzh_CN
dc.subjectamino alcoholszh_CN
dc.subjectasymmetric catalysiszh_CN
dc.subjectcopperzh_CN
dc.subjectHenry reactionzh_CN
dc.subjectmechanistic studyzh_CN
dc.titleHighly Enantioselective Henry Reactions of Aromatic Aldehydes Catalyzed by an Amino Alcohol-Copper(II) Complexzh_CN
dc.typeArticlezh_CN


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