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

Jung Nam Park, Soo Y. Ko, Hun Y. Koh

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

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.

Original languageEnglish
Pages (from-to)5553-5556
Number of pages4
JournalTetrahedron Letters
Volume41
Issue number29
DOIs
StatePublished - 15 Jul 2000

Bibliographical note

Funding Information:
This work was supported by the MOST through the National R&D Program for Women's Universities (Project No. 99-N6-01-01-A-08), and by the KOSEF (1999-2-122-002-4). J.N.P. is grateful to the Brain Korea 21 project for a graduate fellowship.

Keywords

  • 4-epi-cytoxazone
  • Chloramphenicol
  • Cyclic iminocarbonate rearrangement
  • Enantioselective synthesis
  • Regioselection

Fingerprint

Dive into the research topics of 'Synthetic applications of the cyclic iminocarbonate rearrangement Enantioselective syntheses of chloramphenicol and 4-epi-cytoxazone'. Together they form a unique fingerprint.

Cite this