1186523-50-1Relevant articles and documents
Tropos biphenol derived chiral thiophosphoramide catalysed highly diastereo- and enantioselective michael addition of cyclic ketones to nitro olefins
Lu, Aidang,Wu, Ronghua,Wang, Youming,Zhou, Zhenghong,Wu, Guiping,Fang, Jianxin,Tang, Chuchi
, p. 122 - 127 (2011)
Chirality transfer from (S)-2-(aminomethyl)pyrrolidine to the tropos biphenyl skeleton has been observed in the preparation of a chirally flexible biphenol-derived novel chiral thiophosphoramide to afford exclusively the thermodynamically favoured diaster
Chiral thiophosphoramidate-catalyzed asymmetric michael addition of ketones to nitro olefins
Lu, Aidang,Wu, Ronghua,Wang, Youming,Zhou, Zhenghong,Wu, Guiping,Fang, Jianxin,Tang, Chuchi
supporting information; experimental part, p. 2057 - 2061 (2010/06/13)
A novel type of pyrrolidine-based chiral (thio)phosphoramidates was synthesized. Among them, compound (S,aR)-3d was proven to be an effective bifunctional organocatalyst for the asymmetric Michael addition of ketones to nitro olefins. The corresponding adducts were obtained in good to excellent chemical yields with high levels of diastereo- and enantioselectivities (up to >99:1 dr and 99%ee).