Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts

Chemical Communications : Chem Comm
Yi LiShu-Li You

Abstract

Camphor-derived chiral triazolium salts have been found to be highly efficient for asymmetric intramolecular Michael reactions. With 1-5 mol% of the catalyst, the desired products were obtained in excellent yields, with up to 99% ee.

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Citations

Aug 11, 2011·Chemical Communications : Chem Comm·Li-Hui SunSong Ye
Jan 24, 2015·Nature Chemistry·Craig P JohnstonMartin D Smith
Jan 6, 2016·Chemical Society Reviews·Cyril BorieMalek Nechab
Apr 20, 2018·Chemistry, an Asian Journal·Bishnupada SatpathiS S V Ramasastry
Dec 17, 2014·Chemistry : a European Journal·Zhi-Qin LiangSong Ye
Jul 31, 2013·Angewandte Chemie·Biplab Maji, Herbert Mayr
Apr 17, 2015·Chemistry : a European Journal·Lei WangDieter Enders
May 29, 2020·Chemical Communications : Chem Comm·Ram Subhawan VermaBhoopendra Tiwari
Jul 3, 2020·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Sebastijan RičkoUroš Grošelj
Aug 23, 2020·Materials·Krzysztof DzieszkowskiZbigniew Rafiński
Dec 18, 2010·Chemical Communications : Chem Comm·Teng-Yue JianSong Ye
May 28, 2011·Chemical Reviews·Albert Moyano, Ramon Rios

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