Anomeric Selectivity
Anomeric Selectivity is a chemical principle in carbohydrate chemistry that governs the preferential formation of one anomeric configuration over the other during the cyclization of monosaccharides, distinguished by the stereoelectronic and kinetic factors influencing the attack of the nucleophilic hydroxyl group on the electrophilic carbonyl carbon.
185
Publications
7.1K
Citations
609
Authors
196
Institutions
Publications per year
2017–2026
33
Variants
Anomeric Stereoselectivity
Parents
185
Stereoselective Koenigs–Knorr Glycosylation Catalyzed by Urea
Lifeng Sun, Xiaowei Wu, De‐Cai Xiong et al. · Angewandte Chemie International Edition · 2016 · 129 citations
Pharmacy, Chemistry, Biocatalysis +12
1–5 of 185
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National Institute of Neurological Disorders and Stroke, United States
4 publications · 159 citations
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4
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1–5 of 609
196
University of Konstanz
Konstanz, Germany
9 h-index
26 publications
1.4K citations
Scripps Research Institute
San Diego, United States
5 h-index
25 publications
2.6K citations

University of Georgia
Athens, United States
4 h-index
11 publications
392 citations

King Abdulaziz University
Jeddah, Saudi Arabia
4 h-index
4 publications
146 citations
University of Colorado Boulder
Boulder, United States
4 h-index
15 publications
1.5K citations
University College Dublin
Dublin, Ireland
4 h-index
6 publications
405 citations
George Washington University
Washington, United States
4 h-index
12 publications
477 citations
Darmstadt University of Applied Sciences
Darmstadt, Germany
4 h-index
9 publications
320 citations
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JOC · 27 publications · 1.3K citations
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23 publications · 564 citations
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OL · 13 publications · 587 citations
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JACS · 11 publications · 944 citations
11
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10 publications · 248 citations
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