90562-46-2Relevant articles and documents
Thio-Michael addition of α,β-unsaturated amides catalyzed by Nmm-based ionic liquids
Liu, Yawei,Lai, Zhenzhen,Yang, Pengkun,Xu, Yuanqing,Zhang, Wenkai,Liu, Baoying,Lu, Minghua,Chang, Haibo,Ding, Tao,Xu, Hao
, p. 43104 - 43113 (2017)
A simple and practical thio-Michael addition of α,β-unsaturated amides catalyzed by Nmm-based ionic liquids with a 1,2-propanediol group has been developed. All the α,β-unsaturated amides without substituents at the carbon end could smoothly react with su
Study of the Michael addition of β-cyclodextrin-thiol complexes to conjugated alkenes in water
Krishnaveni, N. Srilakshmi,Surendra,Rao, K. Rama
, p. 669 - 671 (2007/10/03)
An environmentally benign and highly efficient supramolecular Michael addition of thiols from the secondary side of β-cyclodextrin to α,β-unsaturated compounds at the primary side in water is described in quantitative yields; products of undesirable side
