{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T19:02:13Z","timestamp":1785438133854,"version":"3.56.0"},"reference-count":36,"publisher":"MDPI AG","issue":"13","license":[{"start":{"date-parts":[[2026,6,24]],"date-time":"2026-06-24T00:00:00Z","timestamp":1782259200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100008043","name":"Zhejiang Sci-Tech University","doi-asserted-by":"crossref","award":["24262237-Y"],"award-info":[{"award-number":["24262237-Y"]}],"id":[{"id":"10.13039\/501100008043","id-type":"DOI","asserted-by":"crossref"}]},{"award":["24262237-Y"],"award-info":[{"award-number":["24262237-Y"]}],"id":[{"id":"https:\/\/ror.org\/03893we55","id-type":"ROR","asserted-by":"publisher"}]},{"name":"Key industrial technology research program of Shaoxing","award":["2024B11016"],"award-info":[{"award-number":["2024B11016"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Molecules"],"abstract":"<jats:p>We report a visible-light-mediated photoreduction strategy for the three-component 1,2-arylpyridylation of alkenes with arylboronic acids and 4-cyanopyridines. The reaction mechanism was verified via radical trapping experiments and DFT calculations. This reaction proceeds under mild conditions, features broad substrate compatibility and is readily scalable to the gram scale.<\/jats:p>","DOI":"10.3390\/molecules31132216","type":"journal-article","created":{"date-parts":[[2026,6,25]],"date-time":"2026-06-25T01:03:56Z","timestamp":1782349436000},"page":"2216","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Visible-Light-Mediated 1,2-Arylpyridylation of Alkenes Using Arylboronic Acids and Cyanopyridines"],"prefix":"10.3390","volume":"31","author":[{"given":"Zi-Wei","family":"Xi","sequence":"first","affiliation":[{"name":"School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhuo-Ying","family":"Dong","sequence":"additional","affiliation":[{"name":"School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shu-Qing","family":"Hu","sequence":"additional","affiliation":[{"name":"School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ke-Li","family":"Qiu","sequence":"additional","affiliation":[{"name":"Shengzhou Innovation Research Institute, Zhejiang Sci-Tech University, Shengzhou 312400, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li","family":"He","sequence":"additional","affiliation":[{"name":"Shengzhou Innovation Research Institute, Zhejiang Sci-Tech University, Shengzhou 312400, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9382-9744","authenticated-orcid":false,"given":"Yong-Miao","family":"Shen","sequence":"additional","affiliation":[{"name":"School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China"},{"name":"Shengzhou Innovation Research Institute, Zhejiang Sci-Tech University, Shengzhou 312400, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2026,6,24]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"4289","DOI":"10.2147\/DDDT.S329547","article-title":"The Expanding Role of Pyridine and Dihydropyridine Scaffolds in Drug Design","volume":"15","author":"Ling","year":"2021","journal-title":"Drug Des. 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