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Total syntheses of tambjamines C, E, F, G, H, I and J, BE-18591 and a related alkaloid from the marine bacterium Pseudoalteromonas tunicata

Date

Authors

Pinkerton, David

Banwell, Martin

Willis, Anthony

Publisher

American Chemical Society

Abstract

The acetate salts of tambjamines C, E, and F (2-4, respectively), as well as those of the related alkaloids BE-18591 (5) and 6, have been prepared by treatment of bipyrrole aldehyde 16 with the relevant amine in the presence of acetic acid. The 5′-bromc

Keywords

Keywords: alkaloid; BE 18591; pyrrole derivative; unclassified drug; article; chemical structure; chemistry; Pseudoalteromonas; stereoisomerism; synthesis; X ray crystallography; Alkaloids; Crystallography, X-Ray; Models, Molecular; Molecular Structure; Pseudoalter

URI

http://hdl.handle.net/1885/38817

Collections

ANU Research Publications

Source

Organic Letters

Type

Journal article

DOI

10.1021/ol7024313

Restricted until

2037-12-31

Downloads

File

Description

01_Pinkerton_Total_syntheses_of_tambjamines_2007.pdf (77.91 KB)

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