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Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines
Liu ZT(刘振婷); Wang YH(王亚辉); Zhu FL(朱付林); Hu XP(胡向平)
Source PublicationORGANIC LETTERS
2016-05-12
Volume18Issue:0Pages:1190
Contribution Rank1
Language英语
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/148365
Collection中国科学院大连化学物理研究所
Corresponding AuthorHu XP(胡向平)
Affiliation大连化学物理研究所
Recommended Citation
GB/T 7714
Liu ZT,Wang YH,Zhu FL,et al. Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines[J]. ORGANIC LETTERS,2016,18(0):1190.
APA 刘振婷,王亚辉,朱付林,&胡向平.(2016).Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines.ORGANIC LETTERS,18(0),1190.
MLA 刘振婷,et al."Enantioselective Copper-Catalyzed Formal [4 + 2] Cycloaddition of o-Aminophenol Derivatives with Propargylic Esters for Synthesis of Optically Active 3,4-Dihydro-2H-1,4-benzoxazines".ORGANIC LETTERS 18.0(2016):1190.
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