Synlett 2000; 2000(9): 1360-1362
DOI: 10.1055/s-2000-7151
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.

Asymmetric Piperidine Synthesis via 1,3-Cyclic Sulfates

Mustafa Eskici* , Timothy Gallagher
  • *School of Chemistry, University of Bristol, Bristol BS8 1TS UK
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Cyclic sulfates undergo a double alkylation with stabilized C,N-dianions derived from 3a/b to provide the piperidine ring system. The 4-substituted variant 7 affords a formal but stereochemically efficient synthesis of (S)-coniine.

    >