204510-90-7Relevant academic research and scientific papers
Reverse-CD mimics with flexible linkages offer adaptable cavity sizes for guest encapsulation
Pathigoolla, Atchutarao,Sureshan, Kana M.
supporting information, p. 317 - 319 (2014/01/06)
Reverse-CD mimics with adaptable cavity sizes have been synthesized. The adaptability has been demonstrated through single crystal structure determination and guest binding studies.
Topochemical click reaction: Spontaneous self-stitching of a monosaccharide to linear oligomers through lattice-controlled azide-alkyne cycloaddition
Pathigoolla, Atchutarao,Gonnade, Rajesh G.,Sureshan, Kana M.
, p. 4362 - 4366 (2012/06/29)
No activation needed: A topochemical click reaction that dispenses with catalyst, solvent, or other modes of activation takes place in crystals of a sugar derivative. The spontaneous, regiospecific azide-alkyne cycloaddition gives linear polymers that are difficult to synthesize by conventional solution-state chemistry (see picture). Copyright
Oligosaccharide synthesis
-
, (2008/06/13)
The invention provides a system for solid-phase synthesis of oligosaccharides, based on the discovery that a 2-substituted-1,3-dioxocycloalkyl linker group of general formula (I) can be used to couple saccharide groups of both the O-glycoside and N-glycos
A galabiose-based two-dimensional scaffold for the synthesis of inhibitors targeting Pk- and P-antigen binding proteins
Ohlsson, J?rgen,Nilsson, Ulf J.
, p. 2785 - 2787 (2007/10/03)
A disaccharide scaffold based on galabiose (Galα1-4Gal) was synthesized. Four different acceptors were evaluated in the α-galactosylation and a relationship between the nucleophilicity, yield, and α/β-selectivity was found. The scaffold contains two ortho
