A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Bibliographic citation
-
A new synthetic access to 2-N-(glycosyl)thiosemicarbazides from 3-N-(glycosyl)oxadiazolinethiones and the regioselectivity of the glycosylation of their oxadiazolinethione precursors ; volume:9 ; pages:135-146
Beilstein journal of organic chemistry ; 9, 135-146
- Classification
-
Chemie
- DOI
-
10.3762/bjoc.9.16
- URN
-
urn:nbn:de:101:1-2013041713630
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:56 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.
Other Objects (12)
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Metal-free glycosylation with glycosyl fluorides in liquid SO2
Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
Zinc Acetate Catalyzed Stereoselective 1,2-trans-Glycosylation Using Glycosyl Chlorides
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthese von C-Glycosyl-Heterocyclen
Rapid glycoconjugation with glycosyl amines
Bimodal Glycosyl Donors as an Emerging Approach Towards a General Glycosylation Strategy
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Metal-free glycosylation with glycosyl fluorides in liquid SO2
Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
Zinc Acetate Catalyzed Stereoselective 1,2-trans-Glycosylation Using Glycosyl Chlorides
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthese von C-Glycosyl-Heterocyclen
Rapid glycoconjugation with glycosyl amines
Bimodal Glycosyl Donors as an Emerging Approach Towards a General Glycosylation Strategy
Diversification of Glycosyl Compounds via Glycosyl Radicals
Diversification of Glycosyl Compounds via Glycosyl Radicals
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity
N-Aryl-O-glycosyl Haloacetimidates as Glycosyl Donors
Metal-free glycosylation with glycosyl fluorides in liquid SO2
Characterization of glycosyl dioxolenium ions and their role in glycosylation reactions
Zinc Acetate Catalyzed Stereoselective 1,2-trans-Glycosylation Using Glycosyl Chlorides
Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols
Synthese von C-Glycosyl-Heterocyclen
Rapid glycoconjugation with glycosyl amines