Exoanomeric Effect
The exoanomeric effect is a stereoelectronic phenomenon in carbohydrate conformation whereby the preference for a specific orientation of the exocyclic C–O bond at the anomeric center arises due to hyperconjugative stabilization between the lone pair on the ring oxygen and the antibonding orbital of the adjacent C–O bond.
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2017–2026
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Exo-anomeric Effect
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Igor Tvaroška, Tibor Kožár · Journal of the American Chemical Society · 1980 · 91 citations
Pharmacy, Biochemistry, Chemistry +17
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Polymer Institute of the Slovak Academy of Sciences, Slovakia
2 publications · 98 citations
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Slovak Academy of Sciences
Bratislava, Slovakia
3 h-index
3 publications
91 citations

Universidad de La Laguna
San Cristóbal de La Laguna, Spain
1 h-index
1 publications
17 citations
National Research Council Canada
Ottawa, Canada
1 h-index
1 publications
61 citations
ETH Zurich
Zurich, Switzerland
1 h-index
1 publications
84 citations
Simon Fraser University
Burnaby, Canada
1 h-index
1 publications
36 citations
Université de Montréal
Montreal, Canada
1 h-index
1 publications
66 citations
United States Department of Agriculture
Washington, United States
1 h-index
1 publications
102 citations
Institute of Chemistry of the Slovak Academy of Sciences
Bratislava, Slovakia
1 h-index
1 publications
46 citations
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8 publications · 544 citations
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JACS · 3 publications · 261 citations
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3 publications · 122 citations
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3 publications · 91 citations
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JBC · 1 publications · 65 citations
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