%0 Journal Article %T The Domino Hexadehydro-Diels-Alder Reaction An Elegant Way toward Polyacenes %+ Institut des Sciences Chimiques de Rennes (ISCR) %A Trolez, Y. %< avec comité de lecture %@ 2451-9294 %J Chem %I Cell Press %V 4 %N 10 %P 2272-2274 %8 2018-10 %D 2018 %R 10.1016/j.chempr.2018.09.021 %Z Chemical Sciences/Organic chemistryJournal articles %X Recently in Nature Chemistry, Xiao and Hoye showed that it is possible to use hexadehydro-Diels-Alder (HDDA) reactions in a domino process to access functionalized polyacenes in high yields. They employed up to four consecutive HDDA reactions to build new highly conjugated polyaromatic molecules. Recently in Nature Chemistry, Xiao and Hoye showed that it is possible to use hexadehydro-Diels-Alder (HDDA) reactions in a domino process to access functionalized polyacenes in high yields. They employed up to four consecutive HDDA reactions to build new highly conjugated polyaromatic molecules. %G English %2 https://univ-rennes.hal.science/hal-01905107/document %2 https://univ-rennes.hal.science/hal-01905107/file/Trolez_The%20Domino%20Hexadehydro-Diels-Alder%20Reaction.pdf %L hal-01905107 %U https://univ-rennes.hal.science/hal-01905107 %~ UNIV-RENNES1 %~ CNRS %~ INSA-RENNES %~ ENSC-RENNES %~ ISCR %~ SCR-COS %~ STATS-UR1 %~ UR1-SPM %~ INC-CNRS %~ UR1-UFR-SPM %~ UR1-HAL %~ ISCR-CORINT %~ UR1-SDLM %~ TEST-UR-CSS %~ UNIV-RENNES %~ INSA-GROUPE %~ ISCR-CORINT2 %~ TEST-HALCNRS %~ UR1-MMS %~ ISCR-CORINT3 %~ TEST2-HALCNRS