Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus)

doi:10.1186/1860-5397-4-6

Beilstein Journal of Organic Chemistry
Volume 4

Viewing options:

Abstract
Full text
PDF (600KB)
Additional files

Associated material:

Related literature:

Articles citing this article
on Google Scholar
on ISI Web of Science
on PubMed Central
Other articles by authors
on Google Scholar

Nelson A
Garraffo HM
Spande TF
Daly JW
Stevenson PJ

on PubMed

Nelson A
Garraffo HM
Spande TF
Daly JW
Stevenson PJ
Related articles/pages
on Google

on Google Scholar

on PubMed

Tools:

Post to:

This article is part of a series on Indolizidines and quinolizidines: natural products and beyond, edited by Prof Joseph P Michael, University of Witwatersrand.

Full Research Paper

Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus)

Angela Nelson¹, H Martin Garraffo², Thomas F Spande², John W Daly² and Paul J Stevenson¹

¹School of Chemistry and Chemical Engineering, Queens University, Belfast, BT9 5AG, Northern Ireland

²Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0820, USA

Beilstein Journal of Organic Chemistry 2008, 4:6doi:10.1186/1860-5397-4-6


Published:	21 January 2008

Additional files

Additional file 1:

Experimental. Details of experimental procedures and data for characterisation of new compounds.

Format: DOC Size: 71KB Download file

This file can be viewed with: Microsoft Word Viewer