ArticleBeilstein journal of organic chemistry2012
2-Allylphenyl glycosides as complementary building blocks for oligosaccharide and glycoconjugate synthesis.
Article in Beilstein journal of organic chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
9 citing papers in PubMed.
- Article
- Cooperatively Catalyzed Activation of Thioglycosides with Iodine and Iron(III) Trifluoromethanesulfonate.Molecules (Basel, Switzerland) · 2025Article
- Ferric Chloride Promoted Glycosidation of Alkyl Thioglycosides.Molecules (Basel, Switzerland) · 2024Article
- HPLC-Based Automated Synthesis of Glycans in Solution.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Palladium(II)-assisted activation of thioglycosides.Organic & biomolecular chemistry · 2021Article
- A Highly Efficient Glycosidation of Glycosyl Chlorides by Using Cooperative Silver(I) Oxide-Triflic Acid Catalysis.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
- S-Benzimidazolyl (SBiz) Imidates as a Platform for Oligosaccharide Synthesis via Active-Latent, Armed-Disarmed, Selective, and Orthogonal Activations.The Journal of organic chemistry · 2017Article
- Templated Oligosaccharide Synthesis: The Linker Effect on the Stereoselectivity of Glycosylation.Organic letters · 2016Article
- Multivalent glycosystems for nanoscience.Beilstein journal of organic chemistry · 2014Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
The O-allylphenyl (AP) anomeric moiety was investigated as a new leaving group that can be activated for chemical glycosylation under a variety of conditions, through both direct and remote pathways. Differentiation between the two activation pathways was achieved in a mechanistic study. The orthogonal-type activation of the AP moiety along with common thioglycosides allows for the execution of efficient oligosaccharide assembly.
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Registered trials
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