%0 Journal Article %T Access to Fused Pyrroles from Cyclic 1,3-Dienyl Boronic Esters and Arylnitroso Compounds %+ Institut des Sciences Chimiques de Rennes (ISCR) %+ Durham University %A Francois, Benjamin %A Eberlin, Ludovic %A Berrée, Fabienne %A Whiting, Andrew %A Carboni, Bertrand %Z Association Nationale de la Recherche et de la Technologie %Z Ministère de l'Éducation Nationale %Z Centre National de la Recherche Scientifique %Z Région Bretagne %< avec comité de lecture %@ 0022-3263 %J Journal of Organic Chemistry %I American Chemical Society %V 85 %N 8 %P 5173-5182 %8 2020 %D 2020 %R 10.1021/acs.joc.9b03214 %M 32192328 %Z Chemical Sciences %Z Chemical Sciences/Organic chemistryJournal articles %X Complimentary to classical hydroboration and boron-Wittig reactions, a new, efficient access to cyclic 1,3-dienyl boronic esters has been developed via diene or triene metathesis. Subsequently, fused pyrroles were synthesized with a broad substrate scope from the reaction of cyclic 1,3-dienyl boronic esters with arylnitroso compounds using a one-pot hetero-Diels-Alder/ring contraction sequence. %G English %2 https://univ-rennes.hal.science/hal-02563405/document %2 https://univ-rennes.hal.science/hal-02563405/file/Fran%C3%A7ois%20et%20al-2020-Access%20to%20Fused%20Pyrroles%20from%20Cyclic%201%2C3-Dienyl%20Boronic%20Esters%20and%20Arylnitroso.pdf %L hal-02563405 %U https://univ-rennes.hal.science/hal-02563405 %~ UNIV-RENNES1 %~ CNRS %~ INSA-RENNES %~ ENSC-RENNES %~ ISCR %~ SCR_ICMV %~ STATS-UR1 %~ UR1-SPM %~ INC-CNRS %~ UR1-UFR-SPM %~ UR1-HAL %~ ISCR-CORINT %~ UR1-SDLM %~ TEST-UR-CSS %~ UNIV-RENNES %~ INSA-GROUPE %~ ISCR-CORINT1 %~ TEST-HALCNRS %~ UR1-MMS %~ TEST2-HALCNRS