1047990-79-3Relevant academic research and scientific papers
The development of an aza-C-glycoside library based on a tandem staudinger/aza-wittig/ugi three-component reaction
Wennekes, Tom,Bonger, Kimberly M.,Vogel, Katrin,Van Den Berg, Richard J. B. H. N.,Van Der Marel, Gijsbert A.,Overkleeft, Herman S.,Strijland, Anneke,Donker-Koopman, Wilma E.,Aerts, Johannes M. F. G.
, p. 6420 - 6454,35 (2020/09/16)
We report the tandem Staudinger/aza-Wittig/Ugi three-component reaction mediated synthesis of a 64-member compound library of aza-C-glycosides. The library is composed of four pyrrolidine and three piperidine scaffolds, onto which a number of functional groups is grafted to form seven sublibraries. Variation in the library is achieved by transformation of two pentoses and a hexose into the corresponding 4-azidopentanal and 5-azidohexanal derivatives as precursors for the Staudinger/aza-Wittig process. Further variation is achieved by using different isocyanides as well as protective- and functional-group manipulations on the fully protected Ugi-3CR intermediates. Preliminary biological evaluation of the compound library revealed several low micromolar inhibitors of human acid glucosylceramidase.
The effect of Lewis acids on the stereochemistry in the Ugi three-component reaction with D-lyxo-pyrroline
Bonger, Kimberly M.,Wennekes, Tom,Filippov, Dmitri V.,Lodder, Gerrit,Van Der Marel, Gijsbert A.,Overkleeft, Herman S.
experimental part, p. 3678 - 3688 (2009/05/07)
A library of polyhydroxylated pyrrolidines was obtained by performing a tandem Staudinger/aza-Wittig/Ugi three-component reaction on a L-ribose-derived 4-azido aldehyde. In this paper we describe the effect of Lewis acids on the diastereoselectivity of th
