- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Comparison of glycosyl donors: a supramer approach ; volume:20 ; year:2024 ; pages:181-192
Beilstein journal of organic chemistry ; 20 (2024), 181-192
- Creator
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Orlova, Anna V.
Malysheva, Nelly N.
Panova, Maria V.
Podvalnyy, Nikita M.
Medvedev, Michael G.
Kononov, Leonid O.
- DOI
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10.3762/bjoc.20.18
- URN
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urn:nbn:de:101:1-2409261447350.438261094685
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Orlova, Anna V.
- Malysheva, Nelly N.
- Panova, Maria V.
- Podvalnyy, Nikita M.
- Medvedev, Michael G.
- Kononov, Leonid O.
Other Objects (12)
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Benzyne arylation of oxathiane glycosyl donors
Bimodal Glycosyl Donors as an Emerging Approach Towards a General Glycosylation Strategy
Reversal of Anomeric Selectivity with O-Glycosyl Trichloroacetimidates as Glycosyl Donors and Thiols as Acceptors Under Acid/Base Catalysis
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Efficient α-Mannosylation of Phenols: The Role of Carbamates as Scavengers for Activated Glycosyl Donors
Investigation of Neighboring Group Participation in 3,4‐Diacetylated Glycosyl Donors in the Gas Phase
Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthesis and Evaluation of Glycosyl Luciferins
Synthese von C-Glycosyl-Heterocyclen
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Benzyne arylation of oxathiane glycosyl donors
Bimodal Glycosyl Donors as an Emerging Approach Towards a General Glycosylation Strategy
Reversal of Anomeric Selectivity with O-Glycosyl Trichloroacetimidates as Glycosyl Donors and Thiols as Acceptors Under Acid/Base Catalysis
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Efficient α-Mannosylation of Phenols: The Role of Carbamates as Scavengers for Activated Glycosyl Donors
Investigation of Neighboring Group Participation in 3,4‐Diacetylated Glycosyl Donors in the Gas Phase
Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthesis and Evaluation of Glycosyl Luciferins
Synthese von C-Glycosyl-Heterocyclen
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Benzyne arylation of oxathiane glycosyl donors
Bimodal Glycosyl Donors as an Emerging Approach Towards a General Glycosylation Strategy
Reversal of Anomeric Selectivity with O-Glycosyl Trichloroacetimidates as Glycosyl Donors and Thiols as Acceptors Under Acid/Base Catalysis
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Efficient α-Mannosylation of Phenols: The Role of Carbamates as Scavengers for Activated Glycosyl Donors
Investigation of Neighboring Group Participation in 3,4‐Diacetylated Glycosyl Donors in the Gas Phase
Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthesis and Evaluation of Glycosyl Luciferins