Electrochemistry
Online ISSN : 2186-2451
Print ISSN : 1344-3542
ISSN-L : 1344-3542
Articles
Electroauxiliary-Assisted Sequential Introduction of Organic Groups on the α-Carbons of Nitrogen
Seiji SUGAMitsuru WATANABEChun-Hong SONGJun-ichi YOSHIDA
Author information
JOURNALS FREE ACCESS

2006 Volume 74 Issue 8 Pages 672-679

Details
Abstract

A method for sequential introduction of two organic groups on the same or the different α-carbons of nitrogen has been developed based on a combination of the concept of electroauxiliary and the cation pool method. Selective introduction of two carbon nucleophiles into 2,5- or 2,2-position of pyrrolidine has been accomplished via sequential electrochemical oxidation of pyrrolidine derivatives containing two silyl groups as the electroauxiliaries. Introduction of two carbon nucleophiles into 2,6-position of piperidine was also successful. The products having two olefinic groups were effectively converted to nitrogen-containing spiro compounds using ring closing metathesis, and an application to formal synthesis of cephalotaxine was also carried out. These results clearly illustrate the synthetic utility and potential of the present approach, and open a new aspect of the synthesis of nitrogen-containing compounds.

Information related to the author
© 2006 The Electrochemical Society of Japan
Previous article Next article
feedback
Top