Park, JN Ko, SY Koh, HY 2024-01-21T13:41:38Z 2024-01-21T13:41:38Z 2021-09-05 2000-07-15 0040-4039 https://pubs.kist.re.kr/handle/201004/141227 Chloramphenicol and 4-epi-cytoxazone have been enantioselectively synthesized using the asymmetric dihydroxylation and the cyclic iminocarbonate rearrangement as key steps. (C) 2000 Elsevier Science Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD BETA-AMINO ACIDS CYTOKINE MODULATOR ASYMMETRIC AMINOHYDROXYLATION CYTOXAZONE DIHYDROXYLATION Synthetic applications of the cyclic iminocarbonate rearrangement: enantioselective syntheses of chloramphenicol and 4-epi-cytoxazone Article 10.1016/S0040-4039(00)00878-9 1 TETRAHEDRON LETTERS, v.41, no.29, pp.5553 - 5556 TETRAHEDRON LETTERS 41 29 5553 5556 scie scopus 000088200200025 2-s2.0-0000862806 Chemistry, Organic Chemistry Article BETA-AMINO ACIDS CYTOKINE MODULATOR ASYMMETRIC AMINOHYDROXYLATION CYTOXAZONE DIHYDROXYLATION enantioselective synthesis cyclic iminocarbonate rearrangement regioselection chloramphenicol 4-epi-cytoxazone