{"OA_type":"gold","page":"2954-2959","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1039/D2SC06952K"}],"volume":14,"doi":"10.1039/d2sc06952k","ddc":["540"],"type":"journal_article","license":"https://creativecommons.org/licenses/by-nc/3.0/","oa_version":"Published Version","article_type":"original","date_published":"2023-02-23T00:00:00Z","scopus_import":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","title":"Nitrogen atom insertion into indenes to access isoquinolines","publisher":"Royal Society of Chemistry","month":"02","citation":{"ieee":"P. Finkelstein, J. Reisenbauer, B. B. Botlik, O. Green, A. Florin, and B. Morandi, “Nitrogen atom insertion into indenes to access isoquinolines,” <i>Chemical Science</i>, vol. 14, no. 11. Royal Society of Chemistry, pp. 2954–2959, 2023.","chicago":"Finkelstein, Patrick, Julia Reisenbauer, Bence B. Botlik, Ori Green, Andri Florin, and Bill Morandi. “Nitrogen Atom Insertion into Indenes to Access Isoquinolines.” <i>Chemical Science</i>. Royal Society of Chemistry, 2023. <a href=\"https://doi.org/10.1039/d2sc06952k\">https://doi.org/10.1039/d2sc06952k</a>.","short":"P. Finkelstein, J. Reisenbauer, B.B. Botlik, O. Green, A. Florin, B. Morandi, Chemical Science 14 (2023) 2954–2959.","ista":"Finkelstein P, Reisenbauer J, Botlik BB, Green O, Florin A, Morandi B. 2023. Nitrogen atom insertion into indenes to access isoquinolines. Chemical Science. 14(11), 2954–2959.","mla":"Finkelstein, Patrick, et al. “Nitrogen Atom Insertion into Indenes to Access Isoquinolines.” <i>Chemical Science</i>, vol. 14, no. 11, Royal Society of Chemistry, 2023, pp. 2954–59, doi:<a href=\"https://doi.org/10.1039/d2sc06952k\">10.1039/d2sc06952k</a>.","apa":"Finkelstein, P., Reisenbauer, J., Botlik, B. B., Green, O., Florin, A., &#38; Morandi, B. (2023). Nitrogen atom insertion into indenes to access isoquinolines. <i>Chemical Science</i>. Royal Society of Chemistry. <a href=\"https://doi.org/10.1039/d2sc06952k\">https://doi.org/10.1039/d2sc06952k</a>","ama":"Finkelstein P, Reisenbauer J, Botlik BB, Green O, Florin A, Morandi B. Nitrogen atom insertion into indenes to access isoquinolines. <i>Chemical Science</i>. 2023;14(11):2954-2959. doi:<a href=\"https://doi.org/10.1039/d2sc06952k\">10.1039/d2sc06952k</a>"},"pmid":1,"tmp":{"short":"CC BY-NC (3.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc/3.0/legalcode","image":"/images/cc_by_nc.png","name":"Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)"},"DOAJ_listed":"1","article_processing_charge":"Yes","_id":"20761","date_updated":"2025-12-16T11:18:13Z","author":[{"last_name":"Finkelstein","first_name":"Patrick","full_name":"Finkelstein, Patrick"},{"last_name":"Reisenbauer","id":"51d862e9-36ee-11f0-86d3-8534c85a5496","first_name":"Julia","full_name":"Reisenbauer, Julia"},{"first_name":"Bence B.","full_name":"Botlik, Bence B.","last_name":"Botlik"},{"full_name":"Green, Ori","first_name":"Ori","last_name":"Green"},{"last_name":"Florin","first_name":"Andri","full_name":"Florin, Andri"},{"full_name":"Morandi, Bill","first_name":"Bill","last_name":"Morandi"}],"external_id":{"pmid":["36937579"]},"oa":1,"status":"public","day":"23","date_created":"2025-12-09T14:23:59Z","has_accepted_license":"1","year":"2023","quality_controlled":"1","publication":"Chemical Science","intvolume":"        14","issue":"11","publication_identifier":{"eissn":["2041-6539"],"issn":["2041-6520"]},"abstract":[{"text":"We report a convenient protocol for a nitrogen atom insertion into indenes to afford isoquinolines. The reaction uses a combination of commercially available phenyliodine(III) diacetate (PIDA) and ammonium carbamate as the nitrogen source to furnish a wide range of isoquinolines. Various substitution patterns and commonly used functional groups are well tolerated. The operational simplicity renders this protocol broadly applicable and has been successfully extended towards the direct interconversion of cyclopentadienes into the corresponding pyridines. Furthermore, this strategy enables the facile synthesis of 15N labelled isoquinolines, using 15NH4Cl as a commercial 15N source.","lang":"eng"}],"publication_status":"published","extern":"1","language":[{"iso":"eng"}],"OA_place":"publisher"}