Download PDF
Synlett 2000; 2000(8): 1148-1150
DOI: 10.1055/s-2000-6768
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Preparation of Cycloalkanone Oxime Ethers via a Free Radical Acylation Approach

Sunggak Kim* , Namsun Kim, Joo-Yong Yoon, Dong Hyun Oh
  • *Department of Chemistry and Center for Molecular Design and Synthesis, School of Molecular Science (BK21), Korea Advanced Institute of Science and Technology, Taejon 305-701, Korea; Fax + 82-42-869-83 70; E-mail: skim@mail.kaist.ac.kr
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

Radical-mediated annulation approaches for the formation of cycloalkanone oxime ethers are described. Based on radical acylation approaches, α-functionalized cycloalkanone oxime ethers, 1,3- and 1,4-cyclohexanedione oxime ethers are prepared.

radical annulation - radical acylation - cycloalkanone oxime ether - sulfonyl oxime ether