Claudia Bello

Prof. Claudia Bello

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 May 2015 in Angewandte Chemie International Edition
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Journal Article
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CBClaudia Bello
Claudia Bello
SWShuo Wang
Shuo Wang
LMLu Meng
Lu Meng
KMKelley W. Moremen
Kelley W. Moremen
CBChristian Becker
Christian Becker

1 February 2013 in Journal of Molecular Biology
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Journal Article
Closed access
MMMoritz Marcinowski
Moritz Marcinowski
MRMathias Rosam
Mathias Rosam
CSChristine Seitz
Christine Seitz
JEJohannes Elferich
Johannes Elferich
JBJulia Behnke
Julia Behnke
JBJohannes Buchner
Johannes Buchner

17 January 2008 in ChemBioChem
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Journal Article
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HLHongqing Li
Hongqing Li
TLTao Liu
Tao Liu
YZYongmin Zhang
Yongmin Zhang
SFSylvain Favre
Sylvain Favre
CBClaudia Bello
Claudia Bello
YBYves Blériot
Yves Blériot

25 August 2010 in European Journal of Organic Chemistry
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Journal Article
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CBClaudia Bonaccini
Claudia Bonaccini
MCMatteo Chioccioli
Matteo Chioccioli
Camilla ParmeggianiCamilla Parmeggiani
Camilla Parmeggiani
Francesca CardonaFrancesca Cardona
Francesca Cardona
DRDaniele Lo Re
Daniele Lo Re
Paola GratteriPaola Gratteri
Paola Gratteri

1 August 2009 in Bioorganic & Medicinal Chemistry
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Journal Article
Closed access
HLHongqing Li
Hongqing Li
FMFilipa Marcelo
Filipa Marcelo
CBClaudia Bello
Claudia Bello
PVPierre Vogel
Pierre Vogel
TBTerry D. Butters
Terry D. Butters
YBYves Blériot
Yves Blériot

3 February 2009 in Organic & Biomolecular Chemistry
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Journal Article
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EMElena Moreno-Clavijo
Elena Moreno-Clavijo
ACAna Teresa Carmona
Ana Teresa Carmona
YVYolanda Vera-Ayoso
Yolanda Vera-Ayoso
AMAntonio J. Moreno-Vargas
Antonio J. Moreno-Vargas
CBClaudia Bello
Claudia Bello
IRInmaculada Robina
Inmaculada Robina
The stereoselective synthesis of new 3,4-dihydroxypyrrolidine derivatives starting from D-mannose, D-ribose and L-fucose is presented. Two synthetic strategies employing organometallic addition to hemiacetalic sugars followed by selective nucleophilic displacement or conjugate addition of ammonia to conjugate aldonic esters as key steps, are used. The new compounds were assayed for their inhibitory activity towards 13 commercially available glycosidases. Compounds that share the absolute configuration at C(2,3,4,5) of L-fucopyranosides and incorporate aromatic moieties are potent and selective inhibitors of α-L-fucosidases in the nM range.