A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction
10.1002/chem.201202504
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sg-nus-scholar.10635-929452024-11-08T19:34:56Z A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction Dou, X. Zhong, F. Lu, Y. CHEMISTRY asymmetric synthesis domino reaction Feist-Bénary reaction organocatalysis synthetic methods 10.1002/chem.201202504 Chemistry - A European Journal 18 44 13945-13948 CEUJE 2014-10-16T08:18:34Z 2014-10-16T08:18:34Z 2012-10-29 Article Dou, X., Zhong, F., Lu, Y. (2012-10-29). A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction. Chemistry - A European Journal 18 (44) : 13945-13948. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.201202504 09476539 http://scholarbank.nus.edu.sg/handle/10635/92945 000310473900004 Scopus |
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asymmetric synthesis domino reaction Feist-Bénary reaction organocatalysis synthetic methods |
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asymmetric synthesis domino reaction Feist-Bénary reaction organocatalysis synthetic methods Dou, X. Zhong, F. Lu, Y. A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
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10.1002/chem.201202504 |
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CHEMISTRY |
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CHEMISTRY Dou, X. Zhong, F. Lu, Y. |
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Dou, X. Zhong, F. Lu, Y. |
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Dou, X. |
title |
A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
title_short |
A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
title_full |
A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
title_fullStr |
A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
title_full_unstemmed |
A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction |
title_sort |
highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified feist-bénary reaction |
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2014 |
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http://scholarbank.nus.edu.sg/handle/10635/92945 |
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