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Self-promoted and stereospecific formation of
N
-glycosides
Michael Martin Nielsen
, Patrycja Mala, Eirikur Þórir Baldursson ,
Christian Marcus Pedersen
Department of Chemistry
Department of Chemistry
9
Citations (Scopus)
3
Downloads (Pure)
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N
-glycosides'. Together they form a unique fingerprint.
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Keyphrases
Self-promotion
100%
Stereospecific
100%
Trichloroacetimidate
83%
Glycosyl Donor
33%
Sulfonamides
33%
Glycosylation
33%
Stereospecificity
33%
Stereoselectivity
33%
Carbamate
33%
Protective Group
33%
Acidic Conditions
16%
Ion Pairs
16%
Popular
16%
NMR Experiments
16%
N-functionalization
16%
GlcNAc
16%
NMR Studies
16%
Glucosyl
16%
Ambient Conditions
16%
Glucosyl Donor
16%
N-glucosides
16%
Tyrosine
16%
Sulfonyl Group
16%
N-glycosylation
16%
Anomer
16%
Gram-scale
16%
Side Chain
16%
Chemistry
formation
100%
Glycoside
100%
Donor
75%
Glycosylation
75%
NMR Spectroscopy
50%
Sulfonamide
50%
Carbamate
50%
Protective
50%
Drop
25%
Acidic Condition
25%
Sulfonyl Group
25%
Stereoselectivity
25%
Ion Pair
25%
Glucoside
25%
Mutarotation
25%
Biochemistry, Genetics and Molecular Biology
Glycosyl
100%
Glycoside
100%
Glycosylation
75%
Promoter Region
50%
Stereospecificity
50%
Sulfonamide
50%
Stereoselectivity
25%
Sulfonyl
25%
Mutarotation
25%
Glucoside
25%
Tyrosine
25%
Anomer
25%