Nitrile Oxide Cycloaddition
Nitrile Oxide Cycloaddition is a bioorthogonal reaction that belongs to the class of 1,3-dipolar cycloadditions, distinguished by the selective and catalyst-free formation of isoxazoline adducts through the interaction of a nitrile oxide dipole with a dipolarophilic alkene or alkyne under physiological conditions.
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2017–2026
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Oxidation of Oximes to Nitrile Oxides with Hypervalent Iodine Reagents
Brian A. Mendelsohn, Shelley Lee, Simon Kim et al. · Organic Letters · 2009 · 214 citations
Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions
Shuji Kanemasa · Synlett · 2002 · 206 citations
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Kyushu University
Fukuoka, Japan
17 h-index
62 publications
1.8K citations
University of Pittsburgh
Pittsburgh, United States
17 h-index
38 publications
1.5K citations

Centre National de la Recherche Scientifique
Paris, France
15 h-index
48 publications
1.3K citations

University of Milan
Milan, Italy
13 h-index
54 publications
1.2K citations
ETH Zurich
Zurich, Switzerland
13 h-index
39 publications
2.5K citations
The University of Tokyo
Tokyo, Japan
12 h-index
34 publications
922 citations
University of Pavia
Pavia, Italy
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42 publications
1.5K citations
University of California, Davis
Davis, United States
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59 publications
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JOC · 90 publications · 4K citations
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OL · 44 publications · 2.3K citations
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JACS · 21 publications · 3.7K citations
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