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Monos\n                    <jats:italic>et al.<\/jats:italic>\n                    present a method that delivers the carbon and nitrogen components in a single reagent, specifically, an aryl ring tethered through sulfur dioxide to an amide. A light-activated catalyst primes an olefin to react with the nitrogen, which in turn leads to migration of the aryl ring and loss of the sulfur bridge. The efficient room-temperature process is applicable to a variety of different arenes, including heterocycles.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Science<\/jats:italic>\n                    , this issue p.\n                    <jats:related-article xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"doi\" issue=\"6409\" page=\"1369\" related-article-type=\"in-this-issue\" vol=\"361\" xlink:href=\"10.1126\/science.aat2117\">1369<\/jats:related-article>\n                  <\/jats:p>","DOI":"10.1126\/science.aat2117","type":"journal-article","created":{"date-parts":[[2018,10,3]],"date-time":"2018-10-03T04:49:24Z","timestamp":1538542164000},"page":"1369-1373","source":"Crossref","is-referenced-by-count":355,"title":["Arylsulfonylacetamides as bifunctional reagents for alkene aminoarylation"],"prefix":"10.1126","volume":"361","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0599-1566","authenticated-orcid":true,"given":"Timothy M.","family":"Monos","sequence":"first","affiliation":[{"name":"Department of Chemistry, University of Michigan, Ann Arbor, MI, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4879-3583","authenticated-orcid":true,"given":"Rory C.","family":"McAtee","sequence":"additional","affiliation":[{"name":"Department of Chemistry, University of Michigan, Ann Arbor, MI, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2443-5514","authenticated-orcid":true,"given":"Corey R. 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