国家自然科学基金(21272227)

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相关期刊:《Chinese Journal of Chemistry》更多>>
相关主题:FLUOROFLUORINATEDESTERSTEREOSELECTIVITYESTERS更多>>
相关领域:理学更多>>
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Formation of Chiral a-Monofluorinated-.8-amino Esters through Organocatalytic Asymmetric Reduction of a-Fluoro-j3-enamino Esters by Trichlorosilane
《Chinese Journal of Chemistry》2012年第11期2636-2640,共5页张鹏 王超 周莉 孙健 
Acknowledgement We are grateful for financial supports from the Na- tional Natural Science Foundation of China (Project Nos. 20972151, 21272227 and 91013006).
A concise method was developed to prepare chiral a-monofluorinated-β-amino esters through N-sulfinyl urea catalyzed asymmetric hydrosilylation of a-fluoro-β-enamino esters, which affords high yields, good to high di...
关键词:asymmetric reduction sulfinyl urea a-fluorinated-β-amino ester STEREOSELECTIVITY 
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