![Regio- and stereoselective 1,3-dipolar cycloaddition reactions of C-aryl (or hetaryl)-N-phenylnitrones to monosubstituted ylidene malononitriles and 4-benzylidene-2-phenyloxazol-5(4H)-one Regio- and stereoselective 1,3-dipolar cycloaddition reactions of C-aryl (or hetaryl)-N-phenylnitrones to monosubstituted ylidene malononitriles and 4-benzylidene-2-phenyloxazol-5(4H)-one](https://www.degruyter.com/document/doi/10.1515/znb-2016-0263/asset/graphic/j_znb-2016-0263_fig_001.jpg)
Regio- and stereoselective 1,3-dipolar cycloaddition reactions of C-aryl (or hetaryl)-N-phenylnitrones to monosubstituted ylidene malononitriles and 4-benzylidene-2-phenyloxazol-5(4H)-one
1,3-Dipolar cycloaddition of nitrones to oxa(aza)bicyclic alkenes - Organic Chemistry Frontiers (RSC Publishing)
![SciELO - Brasil - The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic Acid: Computational Study of Transition States Selectivity, Solvent Effects, and Bicyclo Formation The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic SciELO - Brasil - The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic Acid: Computational Study of Transition States Selectivity, Solvent Effects, and Bicyclo Formation The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic](https://minio.scielo.br/documentstore/1678-4790/8Ynrh9mS9Xz8v3fYDbzq5SM/00283cf27be92fe069894546046c8362eb478996.jpg)
SciELO - Brasil - The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic Acid: Computational Study of Transition States Selectivity, Solvent Effects, and Bicyclo Formation The 1,3-Dipolar Cycloaddition of Nitrile Oxide to Vinylacetic
![The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/cb6da75f-93d9-49d0-9280-755abe69b936/anie202003115-toc-0001-m.jpg)
The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library
![Highly Enantioselective Intramolecular 1,3‐Dipolar Cycloaddition: A Route to Piperidino‐Pyrrolizidines - Vidadala - 2015 - Angewandte Chemie International Edition - Wiley Online Library Highly Enantioselective Intramolecular 1,3‐Dipolar Cycloaddition: A Route to Piperidino‐Pyrrolizidines - Vidadala - 2015 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/573e681f-f675-466f-8dcc-272abbcefeeb/mcontent.jpg)
Highly Enantioselective Intramolecular 1,3‐Dipolar Cycloaddition: A Route to Piperidino‐Pyrrolizidines - Vidadala - 2015 - Angewandte Chemie International Edition - Wiley Online Library
![Diradical-singlet character of 1,3-dipoles affects reactivity of 1,3-dipolar cycloaddition reactions and intramolecular cyclization | SpringerLink Diradical-singlet character of 1,3-dipoles affects reactivity of 1,3-dipolar cycloaddition reactions and intramolecular cyclization | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00894-019-4162-9/MediaObjects/894_2019_4162_Fig1_HTML.png)
Diradical-singlet character of 1,3-dipoles affects reactivity of 1,3-dipolar cycloaddition reactions and intramolecular cyclization | SpringerLink
![The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/ce28bda9-dc80-4d59-9a70-5dc3f58b7129/anie202003115-fig-5001-m.jpg)
The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition - Breugst - 2020 - Angewandte Chemie International Edition - Wiley Online Library
![Catalysts | Free Full-Text | Recent Developments on 1,3-Dipolar Cycloaddition Reactions by Catalysis in Green Solvents | HTML Catalysts | Free Full-Text | Recent Developments on 1,3-Dipolar Cycloaddition Reactions by Catalysis in Green Solvents | HTML](https://www.mdpi.com/catalysts/catalysts-10-00065/article_deploy/html/images/catalysts-10-00065-sch001.png)
Catalysts | Free Full-Text | Recent Developments on 1,3-Dipolar Cycloaddition Reactions by Catalysis in Green Solvents | HTML
![Metal-catalyzed 1,3-dipolar cycloaddition reactions of nitrile oxides - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02072H Metal-catalyzed 1,3-dipolar cycloaddition reactions of nitrile oxides - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB02072H](https://pubs.rsc.org/image/article/2018/OB/c8ob02072h/c8ob02072h-s24_hi-res.gif)