{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T08:40:10Z","timestamp":1789807210580,"version":"4.0.1"},"reference-count":51,"publisher":"Royal Society of Chemistry (RSC)","issue":"59","license":[{"start":{"date-parts":[[2027,6,26]],"date-time":"2027-06-26T00:00:00Z","timestamp":1813968000000},"content-version":"am","delay-in-days":541,"URL":"http:\/\/rsc.li\/journals-terms-of-use"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["24KJB150001"],"award-info":[{"award-number":["24KJB150001"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["rsc.org"],"crossmark-restriction":true},"short-container-title":["Chem. Commun."],"abstract":"<jats:p>\n                    We devised a novel transformation of\n                    <jats:italic>N<\/jats:italic>\n                    -homoallylsulfonyl hydrazones with versatile radical precursors, enabling efficient 1,2-carboimination of unactivated alkenes, accompanied by distinctive 1,4-amino migration.\n                  <\/jats:p>","DOI":"10.1039\/d6cc03098j","type":"journal-article","created":{"date-parts":[[2026,6,26]],"date-time":"2026-06-26T06:43:19Z","timestamp":1782456199000},"page":"14772-14775","update-policy":"https:\/\/doi.org\/10.1039\/rsc_crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Integrating radical deconstruction of the N\u2013N bond in sulfonyl hydrazones and remote 1,4-amino migration to achieve 1,2-carboimination of unactivated alkenes"],"prefix":"10.1039","volume":"62","author":[{"given":"Yi-Feng","family":"Jiang","sequence":"first","affiliation":[{"name":"School of Pharmacy, Changzhou University, Changzhou, Jiangsu 213164, P. 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