Synlett 1998; 1998(9): 981-982
DOI: 10.1055/s-1998-1850
© 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.

Radical Cyclization of N-Aziridinylimines 4. Highly Efficient Synthesis of dl-Pentalenene via Consecutive Carbon-Carbon Bond Formation Approach

Sunggak Kim* , Jae Ho Cheong, Jimmy Yoo
  • *Department of Chemistry, Korea Advanced Institute of Science and Technology, Taejon 305-701, Korea; Fax + 82 42 8 69 58 20; E-mail:
Further Information

Publication History

Publication Date:
31 December 2000 (online)

dl-Pentalenene, an angular triquinane, has been synthesized via tandem radical cyclization of N-aziridinylimine 10 involving the formation of consecutive carbon-carbon bonds.