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Rhamnosylation: diastereoselectivity of conformationally armed donors
Mads Heuckendorff,
Christian Marcus Pedersen
,
Mikael Bols
Department of Chemistry
28
Citations (Scopus)
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Dive into the research topics of 'Rhamnosylation: diastereoselectivity of conformationally armed donors'. Together they form a unique fingerprint.
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Keyphrases
Diastereoselectivity
100%
Glycosylation Reaction
50%
Benzyl
50%
Extremely Low Temperature
50%
Sulfonyl
50%
Increased Temperature
50%
Leaving Group
50%
Electron-withdrawing
50%
Anomer
50%
Excellent Selectivity
50%
Chemistry
Diastereoselectivity
100%
Donor
100%
Benzyl Group
33%
Heterogeneous Catalyst
33%
Glycosylation
33%