Jieun You Han, Jung Tae Jaesook Yun 2026-02-06T08:00:07Z 2026-02-06T08:00:07Z 2026-01-21 2026-01 1861-4728 https://pubs.kist.re.kr/handle/201004/154239 A copper-catalyzed enantioselective hydroboration of cyclic dienes, which afford enantioenriched allylboronates, is disclosed. This reaction is catalyzed by a chiral bisphosphine–Cu complex in combination with commercially available pinacolborane as the hydroborane source. The method is applicable to 1-aryl-cyclohexadienes and 1,2-dihydropyridine derivatives, affording allylboronate products in high regio- and enantioselectivity. The obtained allylboronates serve as versatile intermediates for the synthesis of diverse chiral compounds. English Wiley - V C H Verlag GmbbH & Co. Copper-Catalyzed Asymmetric Hydroboration of Cyclic Dienes Article 10.1002/asia.70555 1 Chemistry - An Asian Journal, v.21, no.1 Chemistry - An Asian Journal 21 1 N scie scopus 001687132900025 Chemistry, Multidisciplinary Chemistry Article ENANTIOSELECTIVE SYNTHESIS 1,4-HYDROBORATION HYDROFUNCTIONALIZATION PINACOLBORANE ALKENES ACCESS copper cyclic dienes enantioselectivity hydroboration regioselectivity