Synlett 1998; 1998(12): 1426-1428
DOI: 10.1055/s-1998-1949
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.

Electron Transfer Driven Addition of Ketimine Derived Radicals to Arene-Cr(CO)3 Complexes

Oliver Hoffmann* , Hans-Günther Schmalz
  • *Institut für Organische Chemie, Sekr. C3, Technische Universität Berlin, Straße des 17. Juni 135, D-10623 Berlin, Germany; Fax + 30 314-2 11 05; E-mail: schmalz@wap0109.chem.tu-berlin.de
Further Information

Publication History

Publication Date:
31 December 2000 (online)

The first examples of SmI2 mediated radical cyclizations of ketimines have been achieved with η 6-arene-Cr(CO)3 complexes bearing ketimine sidechains. The cyclization products were obtained in high yield and with significant diastereoselectivity. The reactions seem to proceed via addition of azaketyl-type radicals to the complexed arenes to form 17 VE intermediates which are trapped by single electron transfer to give the corresponding (anionic) 18 VE species.