Chiral Hydroxytetraphenylene-Catalyzed Asymmetric Conjugate Addition of Boronic Acids to Enones
Publication in refereed journal

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其它資訊
摘要(S)-2,15-Br-2-DHTP-catalyzed asymmetric conjugate addition of boronic acids to beta-trifluoromethyl alpha,beta-unsaturated ketones and enones was studied. The reaction afforded the corresponding Michael addition products in moderate to high yields with excellent enantioselectivities (up to 99:1 er). This catalytic system features mild reaction conditions, high efficiency, and tolerance to heteroarylboronic acids.
出版社接受日期08.05.2019
著者G.-L. Chai, A-Q. Sun, D. Zhai, J. Wang, W.-Q. Deng, H.N.C. Wong, J. Chang
期刊名稱Organic Letters
出版年份2019
月份7
日期5
卷號21
期次13
出版社American Chemical Society
出版地Columbus, Ohio
頁次5040 - 5045
國際標準期刊號1523-7060
電子國際標準期刊號1523-7052
語言美式英語
關鍵詞hydroxytetraphenylene, asymmetric conjugate addition, boronic acid.

上次更新時間 2020-26-10 於 02:37