{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T05:59:30Z","timestamp":1777701570992,"version":"3.51.4"},"reference-count":17,"publisher":"American Chemical Society (ACS)","issue":"9","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Org. 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F.","year":"1999","journal-title":"Angew Chem., Int. Ed."},{"key":"ol0495927b00006\/ol0495927b00006_2","doi-asserted-by":"crossref","first-page":"6343","DOI":"10.1021\/ja020012f","volume":"124","author":"Littke A. F.","year":"2002","journal-title":"J. Am. Chem. Soc."},{"key":"ol0495927b00008\/ol0495927b00008_1","doi-asserted-by":"crossref","first-page":"4295","DOI":"10.1021\/ol016971g","volume":"3","author":"Netherton M. R.","year":"2001","journal-title":"Org. Lett."},{"key":"ol0495927b00009\/ol0495927b00009_1","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1021\/ol006827f","volume":"3","author":"Grasa G. A.","year":"2001","journal-title":"Org. Lett."},{"key":"ol0495927b00010\/ol0495927b00010_1","doi-asserted-by":"crossref","first-page":"14127","DOI":"10.1021\/ja026975w","volume":"124","author":"Choudary B. M.","year":"2003","journal-title":"J. Am. Chem. 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Chem."},{"key":"ol0495927b00014\/ol0495927b00014_1","doi-asserted-by":"crossref","first-page":"7816","DOI":"10.1021\/ja0361493","volume":"125","author":"For Pd\u2212arene","year":"2003","journal-title":"J. Am. Chem. Soc."},{"key":"ol0495927b00016\/ol0495927b00016_1","unstructured":"General Procedure.An oven-dried Schlenk flask equipped with a magnetic stirring bar was charged with Pd2(dba)3(1.5 mol %) and CsF or Me4NF (2.2 mmol) inside a glovebox. If the aryl chloride (1.0 mmol) was a solid, it was also added at this time. The flask was capped with a rubber septum and removed from the glovebox. Ligand1(6.0 mol %) was then added via syringe from a stock solution (2 mM in dioxane). Aryl chloride (if a liquid, 1.0 mmol), tin reagent (1.1 mmol), and dioxane (2 mL) were then successively added via syringe. Under a positive pressure of argon, the flask was sealed with a Teflon screw-cap, and then the reaction mixture was heated at the temperature indicated (see Tables 1\u22123) until the starting material had been completely consumed as judged by TLC. The mixture was then cooled to room temperature, diluted with ether or acetone, filtered, and concentrated in vacuo. The crude product was purified by column chromatography on silica gel."}],"container-title":["Organic Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ol0495927","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,3,14]],"date-time":"2023-03-14T17:09:19Z","timestamp":1678813759000},"score":1,"resource":{"primary":{"URL":"https:\/\/pubs.acs.org\/doi\/10.1021\/ol0495927"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,4,1]]},"references-count":17,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2004,4,1]]}},"alternative-id":["10.1021\/ol0495927"],"URL":"https:\/\/doi.org\/10.1021\/ol0495927","relation":{},"ISSN":["1523-7060","1523-7052"],"issn-type":[{"value":"1523-7060","type":"print"},{"value":"1523-7052","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,4,1]]}}}