Cheong, CS Park, YJA Lee, SH Im, DS Jung, SH 2024-01-21T13:38:31Z 2024-01-21T13:38:31Z 2022-01-11 2000-08 1024-2430 https://pubs.kist.re.kr/handle/201004/141171 3, 4-Disubstituted gamma -lactones 9 and 10 were stereoselectively synthesized from 3,4-unsaturated aliphatic alcohol. The synthetic methods of homoallylic alcohol were discussed. Asymmetric dihydroxylation of the double bond was performed by Sharpless' method with (DHQD)(2)PHAL or (DHQ)(2)PHAL. The stereo-chemistry of the product was assigned. The (3R,4R)- and (3S,4S)-compounds were obtained with high enantiomeric excess. English GORDON BREACH PUBLISHING, TAYLOR & FRANCIS GROUP DIHYDROXYLATION INHIBITION ANALOGS Asymmetric synthesis of biologically useful 3,4-disubstituted gamma-lactone (3,4-Db) Article 1 ENANTIOMER, v.5, no.6, pp.585 - 590 ENANTIOMER 5 6 585 590 scie scopus 000168653700008 2-s2.0-0034440735 Biochemistry & Molecular Biology Chemistry, Multidisciplinary Chemistry, Organic Biochemistry & Molecular Biology Chemistry Article DIHYDROXYLATION INHIBITION ANALOGS cyclohexanedione furane fungicidal agent gamma-lactones