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Pyrrole aminoimidazole alkaloid metabiosynthesis with marine sponges Agelas conifera and Stylissa caribica.
Angew Chem Int Ed Engl. 2012 May 14;51(20):4877-81. doi: 10.1002/anie.201108119. Epub 2012 Apr 4.
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Metabolomics approach to chemical diversity of the Mediterranean marine sponge Agelas oroides.
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A short total synthesis of the marine sponge pyrrole-2-aminoimidazole alkaloid (±)-agelastatin A.
Angew Chem Int Ed Engl. 2013 Oct 4;52(41):10862-6. doi: 10.1002/anie.201304759. Epub 2013 Aug 22.
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Bromosceptrin, an alkaloid from the marine sponge Agelas conifera.
Z Naturforsch C J Biosci. 2002 Jan-Feb;57(1-2):157-60. doi: 10.1515/znc-2002-1-226.
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A submarine journey: the pyrrole-imidazole alkaloids.
Mar Drugs. 2009 Nov 27;7(4):705-53. doi: 10.3390/md7040705.
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Ageladine A, a pyrrole-imidazole alkaloid from marine sponges, is a pH sensitive membrane permeable dye.
Biochem Biophys Res Commun. 2008 Aug 29;373(3):419-22. doi: 10.1016/j.bbrc.2008.06.056. Epub 2008 Jun 25.

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Total Synthesis and Structural Revision of (±)-Mauritamide B.
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Short macrocyclic peptides in sponge genomes.
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Secondary metabolites from marine sponges of the genus : a comprehensive update insight on structural diversity and bioactivity.
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Marine Pyrrole Alkaloids.
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Precursor-Guided Mining of Marine Sponge Metabolomes Lends Insight into Biosynthesis of Pyrrole-Imidazole Alkaloids.
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Total Synthesis of (±)-Sceptrin.
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Total synthesis of all (-)-Agelastatin alkaloids.
Chem Sci. 2010 Jan 1;1:561-566. doi: 10.1039/c0sc00351d.
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Revisiting the Kinnel-Scheuer hypothesis for the biosynthesis of palau'amine.
Chem Commun (Camb). 2011 Jan 7;47(1):427-9. doi: 10.1039/c0cc02214d. Epub 2010 Sep 16.
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Total synthesis of palau'amine.
Angew Chem Int Ed Engl. 2010 Feb 1;49(6):1095-8. doi: 10.1002/anie.200907112.
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Sceptrin, a marine natural compound, inhibits cell motility in a variety of cancer cell lines.
ACS Chem Biol. 2010 Feb 19;5(2):195-202. doi: 10.1021/cb900240k.
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Exploring symmetry-based logic for a synthesis of palau'amine.
J Org Chem. 2009 Aug 21;74(16):5909-19. doi: 10.1021/jo900755r.
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Crossed intermolecular [2+2] cycloadditions of acyclic enones via visible light photocatalysis.
J Am Chem Soc. 2009 Oct 21;131(41):14604-5. doi: 10.1021/ja903732v.

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