DSpace at KIST: Synthetic applications of the cyclic iminocarbonate rearrangement: enantioselective syntheses of chloramphenicol and 4-epi-cytoxazone

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Synthetic applications of the cyclic iminocarbonate rearrangement: enantioselective syntheses of chloramphenicol and 4-epi-cytoxazone

Authors: Park, JN; Ko, SY; Koh, HY

Issue Date: 2000-07-15

Publisher: PERGAMON-ELSEVIER SCIENCE LTD

Citation: TETRAHEDRON LETTERS, v.41, no.29, pp.5553 - 5556

Abstract: 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.

Keywords: BETA-AMINO ACIDS; CYTOKINE MODULATOR; ASYMMETRIC AMINOHYDROXYLATION; CYTOXAZONE; DIHYDROXYLATION; BETA-AMINO ACIDS; CYTOKINE MODULATOR; ASYMMETRIC AMINOHYDROXYLATION; CYTOXAZONE; DIHYDROXYLATION; enantioselective synthesis; cyclic iminocarbonate rearrangement; regioselection; chloramphenicol; 4-epi-cytoxazone

ISSN: 0040-4039

URI: https://pubs.kist.re.kr/handle/201004/141227

DOI: 10.1016/S0040-4039(00)00878-9

Appears in Collections:: KIST Article > 2000

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