PDF herunterladen
Synlett 1997; 1997(9): 1061-1062
DOI: 10.1055/s-1997-1524
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.

An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone

Stéphane Raeppel, Dominique Toussaint, Jean Suffert*
  • *Laboratoire de Pharmacochimie Moléculaire, Centre de Neurochimie du CNRS, UPR 421, 5, rue Blaise Pascal, F-67084 Strasbourg Cedex, France, Fax (33) 3 88 60 08 10; Bitnet jeansu@neurochem.u-strasbg.fr
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 2000 (online)

 als PDF herunterladen  Lizenzen und Reprints Alle Artikel dieser Rubrik

An efficient synthesis of both enantiomers of trans-3,4-bis(benzyloxy)cyclopentanone 4, potential precursors to the five-membered (A)-ring of the neocarzinostatin chromophore, was accomplished from diethyl tartrate in 7 steps.

trans-3,4-bis(benzyloxy)cyclopentanone - diethyl tartrate - TosMIC - neocarzinostatin - kedarcidine