[an error occurred while processing this directive]
Skip to Main Content

Latest News

January 11, 2010
Volume 88, Number 2
p. 5
Article appeared online January 5, 2010

Finally, Palau'amine

Organic Synthesis: Ring formation anchors landmark conquest of complex marine natural product

Carmen Drahl

The Ring's The Thing: Baran's team cemented palau'amine's core in place with a cyclization across a large ring. View Enlarged Image
The Ring's The Thing Baran's team cemented palau'amine's core in place with a cyclization across a large ring.
  • Print this article
  • Email the editor

Latest News

October 28, 2011

Speedy Homemade-Explosive Detector

Forensic Chemistry: A new method could increase the number of explosives detected by airport screeners.

Solar Panel Makers Cry Foul

Trade: U.S. companies complain of market dumping by China.

Novartis To Cut 2,000 Jobs

Layoffs follow similar moves by Amgen, AstraZeneca.

Nations Break Impasse On Waste

Environment: Ban to halt export of hazardous waste to developing world.

New Leader For Lawrence Livermore

Penrose (Parney) Albright will direct DOE national lab.

Hair Reveals Source Of People's Exposure To Mercury

Toxic Exposure: Mercury isotopes in human hair illuminate dietary and industrial sources.

Why The Long Fat?

Cancer Biochemistry: Mass spectrometry follows the metabolism of very long fatty acids in cancer cells.

Text Size A A

With the help of a daring cyclization reaction, a team led by Phil S. Baran at Scripps Research Institute has completed the first total synthesis of palau'amine, a marine natural product that has captivated synthetic chemistry groups around the globe (Angew. Chem. Int. Ed., DOI://10.1002/anie.200907112).

Isolated from the sponge Stylotella agminata in waters near the Pacific Ocean Republic of Palau, palau'amine is a dauntingly complex alkaloid. It has eight contiguous stereogenic centers and a preponderance of reactive nitrogen-containing moieties. It is also highly polar, which can make it nightmarishly difficult to manipulate synthetic intermediates. The challenge of making such a complex structure has intrigued chemists for more than a decade.

Until now, "palau'amine's unprecedented hexacyclic ring system and its nasty physical properties had undermined total synthesis endeavors in leading laboratories worldwide," says Larry E. Overman, an organic chemist at the University of California, Irvine, who has worked on palau'amine and its relatives in the pyrrole-imidazole alkaloid family.

Palau'amine's biggest chemical challenge is in its highly strained core, which features a peculiar trans junction between two five-membered rings. This feature was one of a few recent revisions to palau'amine's structure proposed by an international team in 2007 (C&EN, Mar. 5, 2007, p. 12). That revision was key to finishing the synthesis, but so were a variety of synthetic tenets that are the hallmark of the Baran lab. For instance, en route to palau'amine, the Scripps team harnessed the innate reactivity of nitrogen heterocycles, minimizing the use of protecting groups (C&EN Jun. 4, 2007, p. 38).

After several attempts to make the strained core met with failure, Baran, graduate student Ian B. Seiple, postdoctoral researcher Shun Su, and colleagues tried a different cyclization strategy. They reasoned that a hypothetical molecule with a large ring, which they dubbed "macro-palau'amine", might lead to palau'amine via cyclization across the large ring. Their strategy succeeded, but not until they had explored this line of attack for nearly two years.

Overman says the cyclization step "exemplifies the innovative retrosynthetic analysis and mechanistic thinking that underpins the Baran group's remarkable string of total synthesis successes in this area."

The Scripps team didn't make the natural product via proposed biomimetic cyclizations, notes Daniel Romo of Texas A&M University, who also has worked on this alkaloid family. "Together with their elegant successful strategy, this raises intriguing questions about how palau'amine might really be made in nature."

Baran emphasized that the job isn't done. His team is working on an enantioselective version of the synthesis for obtaining gram scales of material. Even though initial reports of palau'amine's promising biological activity have yet to pan out, the structure and others like it are a fertile testing ground for chemical strategies. "The problem with most news stories about a synthesis is that they give the community a false sense of closure," Baran says. Unless chemists can routinely make large quantities of scarce natural products such as palau'amine for further investigations, the need for chemical innovation is far from over, he says. "I don't see this synthesis as an end--I see this as a beginning."

Chemical & Engineering News
ISSN 0009-2347
Copyright © 2011 American Chemical Society
  • Print this article
  • Email the editor

Services & Tools

ACS Resources

ACS is the leading employment source for recruiting scientific professionals. ACS Careers and C&EN Classifieds provide employers direct access to scientific talent both in print and online. Jobseekers | Employers

» Join ACS

Join more than 161,000 professionals in the chemical sciences world-wide, as a member of the American Chemical Society.
» Join Now!