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Utilizing xanthate esters with an\n                    <jats:italic>S<\/jats:italic>\n                    \u2010allyl substituent leads to higher yields compared to the more commonly used\n                    <jats:italic>S<\/jats:italic>\n                    \u2010Me xanthate esters. The reaction is tolerant toward a wide array of functional groups and allows for the conversion of xanthate esters derived from pharmaceuticals to diarylmethanes. Electronic properties of the reaction partners have a strong influence on the reaction. Mechanistic investigations revealed that the benzylic radical is generated from the xanthate ester, presumably by single electron transfer by Ni(I).\n                  <\/jats:p>","DOI":"10.1002\/chem.71207","type":"journal-article","created":{"date-parts":[[2026,6,7]],"date-time":"2026-06-07T03:49:25Z","timestamp":1780804165000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Nickel\u2010Catalyzed Reductive Cross\u2010Coupling of Xanthate Esters With Aryl and Alkenyl Iodides"],"prefix":"10.1002","volume":"32","author":[{"given":"Felix","family":"V\u00f6hringer","sequence":"first","affiliation":[{"name":"Institute of Organic Chemistry Faculty of Science Eberhard Karls Universit\u00e4t T\u00fcbingen  T\u00fcbingen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kathrin","family":"Zwettler","sequence":"additional","affiliation":[{"name":"Institute of Organic Chemistry Faculty of Science 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