Total Syntheses of Tambjamines C, E, F, G, H, I and J, BE-18591, and a Related Alkaloid from the Marine Bacterium Pseudoalteromonas tunicata-Reference-Cited by-同舟云学术

Total Syntheses of Tambjamines C, E, F, G, H, I and J, BE-18591, and a Related Alkaloid from the Marine Bacterium Pseudoalteromonas tunicata

Published:2007-10-27 Issue:24 Volume:9 Page:5127-5130
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pinkerton David M.¹,Banwell Martin G.¹,Willis Anthony C.¹

Affiliation:

1. Research School of Chemistry, Institute of Advanced Studies, The Australian National University, Canberra, ACT 0200, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol7024313

Reference19 articles.

1. For convenience, and because they each possess the same bipyrrolic core, we have designated all of the natural products1−12as tambjamines even though one of these,5, has been assigned the code-name BE-18591 while another,12, has only been identified as a “.new member of the tambjamine class.” and remains to be given a letter designation.

2. Defensive metabolites from three nembrothid nudibranchs

3. New tamjamine class alkaloids from the marine ascidianAtapozoa sp. and its nudibranch predators. Origin of the tambjamines inAtapozoa

4. A new antitumor substance, BE-18591, produced by a streptomycete. I. Fermentation, isolation, physico-chemical and biological properties.

5. New Tambjamine Alkaloids From the Marine Bryozoan Bugula dentata

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