Synthesis of β-O-glycosides using enol ether and imidate derived leaving groups. Emphasis on the use of nitriles as a solvent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Ergebnisse und Probleme derO-Glykosidsynthese
2. Results and Problems ofO-Glycoside Synthesis
3. Über die orthoesterbildung als konkurrenzreaktion zur glykosylierung
4. On the stereochemical control of glycosylation reactions by the addition of tetrahydrofuran
5. The Application of the Trichloroacetimidate Method to the Synthesis of α-D-Gluco- and α-D-Galactopyranosides
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1. Reaction Rate and Stereoselectivity Enhancement in Glycosidations with O-Glycosyl Trihaloacetimidate Donors due to Catalysis by a Lewis Acid–Nitrile Cooperative Effect;The Journal of Organic Chemistry;2024-05-28
2. Synthesis of Unprecedented α/β‐Alternate (1→4)‐Glucans via Stereoselective Iterative Glycosylation;Chemistry – A European Journal;2023-04-19
3. A Mild Glycosylation Protocol with Glycosyl 1‐Methylimidazole‐2‐carboxylates as Donors;European Journal of Organic Chemistry;2021-07-21
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