42313-51-9Relevant articles and documents
Multivalent thioglycopeptoids via photoclick chemistry: Potent affinities towards LecA and BC2L-A lectins
Caumes,Gillon,Legeret,Taillefumier,Imberty,Faure
supporting information, p. 12301 - 12304 (2015/07/27)
Solution-phase synthesis of linear and cyclic β- and α,β-peptoids was coupled to photo-induced thiol-ene coupling reaction to readily access multivalent thioglycoclusters. A tetrameric cyclic β-peptoid scaffold displaying 1-thio-β-D-galactose or 1-thio-α-D-mannose has revealed by ITC experiments efficient binding potency for bacterial lectins LecA and BC2L-A, respectively.
Complex containing a Lewis acid and Bronsted acid for the catalytic reactions of aza-Michael addition
Mao, Xin-Xin,Wang, Jiao,Xia, Qun-Hua,Shen, Yong-Miao
experimental part, p. 525 - 528 (2011/10/31)
The novel efficient complex catalyst containing a Lewis acid and a Bronsted acid have been prepared by the reaction of proline ion liquid and cuprous iodide. The catalyst was characterized by FT-IR techniques using pyridine as probe molecule. A fast, mild, and quantitative procedure for aza-Michael addition reactions between various amines and α,β- unsaturated carbonyl compounds and nitriles has been developed using the novel complex catalyst. The results showed that the novel catalyst owned high activities for the reactions with excellent yields within 1 min.
Catalyzed synthesis of β-amino acids esters
Dokichev,Latypova,Shakirov,Biglova,Talipov
experimental part, p. 755 - 757 (2010/10/02)
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