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Articles by Simone Di Noja
Progressive endergonic synthesis of Diels‐Alder adducts driven by chemical energy
Supporting Information As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors.
Progressive Endergonic Synthesis of Diels-Alder Adducts Driven by Chemical Energy
Supporting Information As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors.
Photochemical Bromination of 2,5‐Dimethylbenzoic Acid as Key Step of an Improved Alkyne‐Functionalized Blue Box Synthesis
Article Dans Une Revue European Journal of Organic Chemistry Année : 2023 Photochemical Bromination of 2,5‐Dimethylbenzoic Acid as Key Step of an Improved Alkyne‐Functionalized Blue Box Synthesis Origine : Publication financée par une institution hal-04570227 , version 1 (06-05-2024) Ahmad Bachir, Fabiana Ciocchetti, Daniel P. Couto, Simone Di Noja, Cristian Pezzato, et al.. Photochemical Bromination of 2,5‐Dimethylbenzoic Acid as Key Step of an Improved Alkyne‐Functionalized Blue Box Synthesis.
Photochemical Bromination of 2,5‐Dimethylbenzoic Acid as Key Step of an Improved Alkyne‐Functionalized Blue Box Synthesis
Abstract Cyclobis(paraquat-p-phenylene), also known as "blue box", is a highly electron-deficient macrocycle, widely used as a molecular receptor for small electron-rich molecules. Inserting a reactive functional group onto the molecular structure of this cyclophane is paramount for its inclusion into complex architectures. To this aim, including an alkyne moiety would be ideal, because it can participate in click reactions.
Photochemical Bromination of 2,5‐Dimethylbenzoic Acid as Key Step of an Improved Alkyne‐Functionalized Blue Box Synthesis**
Graphical Abstract In this work, the synthesis of an alkyne-functionalized blue box has been revised. Overcoming the limits of the existing synthesis for every single step, the overall yield was increased five times. Importantly, photochemical bromination was adopted to obtain a key intermediate. The target compound was functionalized by using click-chemistry, and it was confirmed by electrochemical techniques that it retains the ability to engage in radical-radical interactions.
Synthesis and applications of amino-functionalized carbon nanomaterials
Synthesis and applications of amino-functionalized carbon nanomaterials Marina Garrido, †a Lorenzo Gualandi,†a Simone Di Noja, a Giacomo Filippini, a Susanna Bosia and Maurizio Prato *abc Author affiliations * Corresponding authors a Department of Chemical and Pharmaceutical Sciences, CENMAT, Center of Excellence for Nanostructured Materials, INSTM UdR, Trieste, University of Trieste, Via Licio Giorgieri 1, Trieste 34127, Italy E-mail: prato@units.it b Center for Cooperative Research in...
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