Song, CE Kim, YH Lee, KC Lee, S Jin, BW 2024-01-21T18:04:36Z 2024-01-21T18:04:36Z 2021-09-04 1997-09-11 0957-4166 https://pubs.kist.re.kr/handle/201004/143593 Using new C-2-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee. (C) 1997 Elsevier Science Ltd. English PERGAMON-ELSEVIER SCIENCE LTD GENERATED IN-SITU DIOXIRANE ALKENES OXAZIRIDINES OXIDATIONS REACTIVITY CHEMISTRY New C-2-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins Article 10.1016/S0957-4166(97)00352-2 1 TETRAHEDRON-ASYMMETRY, v.8, no.17, pp.2921 - 2926 TETRAHEDRON-ASYMMETRY 8 17 2921 2926 scie scopus A1997XY65700009 2-s2.0-0030865630 Chemistry, Inorganic & Nuclear Chemistry, Organic Chemistry, Physical Chemistry Article GENERATED IN-SITU DIOXIRANE ALKENES OXAZIRIDINES OXIDATIONS REACTIVITY CHEMISTRY C//2-symmetric chiral ketones