Iodonium-Promoted Glycosylations with Phenyl Selenoglycosides
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference13 articles.
1. The conversion of 4-oxa-5-hexenyllithiums to 4-alken-1-ols: a novel [1,4]-wittig rearrangement
2. n-Pentenyl glycosides permit the chemospecific liberation of the anomeric center
3. Iodonium ion promoted reactions at the anomeric centre. II An efficient thioglycoside mediated approach toward the formation of 1,2-trans linked glycosides and glycosidic esters
4. An efficient thioglycoside-mediated formation of α-glycosidic linkages promoted by iodonium dicollidine perchlorate
5. Iodonium ion-assisted glycosylation of alkyl (aryl) 1-thio-glycosides: regulation of stereoselectivity and reactivity
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2. β-Glycosylations with 2-Deoxy-2-(2,4-dinitrobenzenesulfonyl)-amino-glucosyl/galactosyl Selenoglycosides: Assembly of Partially N-Acetylated β-(1 → 6)-Oligoglucosaminosides;The Journal of Organic Chemistry;2023-06-12
3. In Situ Preactivation Strategies for the Expeditious Synthesis of Oligosaccharides: A Review;Journal of Carbohydrate Chemistry;2014-07-14
4. A facile method for synthesizing selenoglycosides based on selenium-transfer to glycosyl imidate;Tetrahedron Letters;2014-03
5. Mechanism of Chemical Glycosylation: Focus on the Mode of Activation and Departure of Anomeric Leaving Groups;Journal of Carbohydrate Chemistry;2013-01-01
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