{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,22]],"date-time":"2026-08-22T16:25:10Z","timestamp":1787415910452,"version":"build-2736575974"},"reference-count":27,"publisher":"American Chemical Society (ACS)","issue":"33","license":[{"start":{"date-parts":[[2026,8,10]],"date-time":"2026-08-10T00:00:00Z","timestamp":1786320000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2026,8,10]],"date-time":"2026-08-10T00:00:00Z","timestamp":1786320000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2026,8,10]],"date-time":"2026-08-10T00:00:00Z","timestamp":1786320000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-045"}],"funder":[{"DOI":"10.13039\/501100001843","name":"Science and Engineering Research Board","doi-asserted-by":"publisher","award":["CRG\/2022\/000689"],"award-info":[{"award-number":["CRG\/2022\/000689"]}],"id":[{"id":"10.13039\/501100001843","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004541","name":"Ministry of Education, India","doi-asserted-by":"publisher","award":["NA"],"award-info":[{"award-number":["NA"]}],"id":[{"id":"10.13039\/501100004541","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,8,21]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Herein, we report a reusable UiO-67-Pd catalyst for additive-free transfer hydrogenation of epoxides at room temperature using ammonia borane as the hydrogen source. The protocol enables selective conversion of aromatic and aliphatic epoxides into the corresponding alcohols and can be readily applied to the reduction of other unsaturated functionalities, including \u03b1,\u03b2-unsaturated ketones, N-heterocycles, azoarenes, and nitroarenes. A series of mechanistic investigations were carried out to understand the catalytic process.<\/jats:p>","DOI":"10.1021\/acs.orglett.6c02789","type":"journal-article","created":{"date-parts":[[2026,8,10]],"date-time":"2026-08-10T21:02:11Z","timestamp":1786395731000},"page":"10489-10494","source":"Crossref","is-referenced-by-count":0,"title":["Heterogeneous\nPalladium-Catalyzed Transfer Hydrogenation\nof Epoxide and Structurally Diverse Unsaturated Bonds at Room Temperature"],"prefix":"10.1021","volume":"28","author":[{"given":"Manoj","family":"Pradhan","sequence":"first","affiliation":[{"name":"Indian Institute of Technology Kanpur , , , ,","place":["Kanpur, Uttar Pradesh, India, 208016"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adarsha","family":"Mandal","sequence":"additional","affiliation":[{"name":"Indian Institute of Technology Kanpur , , , ,","place":["Kanpur, Uttar Pradesh, India, 208016"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Liyuan","family":"Qu","sequence":"additional","affiliation":[{"name":"Nagoya University , , , ,","place":["Nagoya, Aichi, Japan, 464-8603"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5368-3157","authenticated-orcid":true,"given":"Hiroaki","family":"Iguchi","sequence":"additional","affiliation":[{"name":"Nagoya University , , , ,","place":["Nagoya, Aichi, Japan, 464-8603"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7665-6212","authenticated-orcid":true,"given":"Ryotaro","family":"Matsuda","sequence":"additional","affiliation":[{"name":"Nagoya University , , , ,","place":["Nagoya, Aichi, Japan, 464-8603"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4227-294X","authenticated-orcid":true,"given":"Sabuj","family":"Kundu","sequence":"additional","affiliation":[{"name":"Indian Institute of Technology Kanpur , , , ,","place":["Kanpur, Uttar Pradesh, India, 208016"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2026,8,10]]},"reference":[{"key":"2026082212103685700_cit1","doi-asserted-by":"publisher","first-page":"8153","DOI":"10.1021\/cr500036t","article-title":"The Chemistry of Transition Metals with Three-Membered\nRing Heterocycles","volume":"114","author":"Huang","year":"2014","journal-title":"Chem. 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A: Chem."},{"key":"2026082212103685700_cit5","doi-asserted-by":"publisher","first-page":"1813","DOI":"10.1246\/bcsj.60.1813","article-title":"Chemo- and Regioselective\nReduction\nof Epoxides with Sodium Borohydride in Mixed Solvent Containing Methanol","volume":"60","author":"Ookawa","year":"1987","journal-title":"Bull. Chem. Soc. Jpn."},{"key":"2026082212103685700_cit6","doi-asserted-by":"publisher","first-page":"2649","DOI":"10.1021\/ja01038a042","article-title":"Reduction of epoxides. III. Lithium\naluminum hydride and mixed hydride reduction of some secondary-tertiary\nepoxides","volume":"91","author":"Murphy","year":"1969","journal-title":"J. Am. Chem. Soc."},{"key":"2026082212103685700_cit7","doi-asserted-by":"publisher","first-page":"1884","DOI":"10.1246\/bcsj.64.1884","article-title":"Selective Ring-Opening Reaction of\nEpoxides with Sodium Borohydride in the Presence of Cyclodextrins\nin Aqueous Media","volume":"64","author":"Hu","year":"1991","journal-title":"Bull. Chem. 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