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Organocatalytic Asymmetric Cycloaddition Reaction of Ketenes
Wang Aie ; Zhang Jinlong ; Wang AE(王爱娥)
刊名http://dx.doi.org/10.6023/cjoc1103301
2012-01
关键词N-HETEROCYCLIC CARBENES HIGHLY ENANTIOSELECTIVE SYNTHESIS AMINO-ACID DERIVATIVES BETA-LACTAMS DISUBSTITUTED KETENES CATALYZED CYCLOADDITION LACTONES DIMERIZATION NUCLEOPHILE IMINES
英文摘要National Natural Science Foundation of China [20902075]; Natural Science Foundation of Fujian Province [2009J05037]; Research Fund for the Doctoral Program of Higher Education of China [20090121120007]; Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry; In this review, organocatalytic asymmetric [2+2] and [4+2] cycloaddition reactions of ketenes are summarized with emphasis on the selectivities and mechanisms of different catalysts.
语种英语
出版者CHINESE J ORG CHEM
内容类型期刊论文
源URL[http://dspace.xmu.edu.cn/handle/2288/88383]  
专题化学化工-已发表论文
推荐引用方式
GB/T 7714
Wang Aie,Zhang Jinlong,Wang AE. Organocatalytic Asymmetric Cycloaddition Reaction of Ketenes[J]. http://dx.doi.org/10.6023/cjoc1103301,2012.
APA Wang Aie,Zhang Jinlong,&王爱娥.(2012).Organocatalytic Asymmetric Cycloaddition Reaction of Ketenes.http://dx.doi.org/10.6023/cjoc1103301.
MLA Wang Aie,et al."Organocatalytic Asymmetric Cycloaddition Reaction of Ketenes".http://dx.doi.org/10.6023/cjoc1103301 (2012).
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