Synlett 2015; 26(07): 937-941
DOI: 10.1055/s-0034-1380151
letter
© Georg Thieme Verlag Stuttgart · New York

Bisnucleophilic Substitution as a Synthetic Tool for Ready Access to the Piperidine Alkaloids (+)-Connine, (+)-β-Conhydrine, (+)-8-Ethylnorlobelol, and (–)-Halosaline

Galla Raju
Organic & Biomolecular Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India   Email: prkgenius@iict.res.in
,
Kadimi Anitha
Organic & Biomolecular Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India   Email: prkgenius@iict.res.in
,
Palakodety Radha Krishna*
Organic & Biomolecular Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India   Email: prkgenius@iict.res.in
› Author Affiliations
Further Information

Publication History

Received: 19 November 2014

Accepted after revision: 14 January 2015

Publication Date:
19 February 2015 (online)


Abstract

Herein we report the stereoselective total synthesis of (+)-connine, (+)-β-conhydrine, (+)-8-ethylnorlobelol, and (–)-halosaline via bisnucleophilic substitution with benzylamine as the key step.

Supporting Information