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- Synthesis and biology of cyclic imine toxins, an emerging class of potent, globally distributed marine toxins. Craig E. Stivala, Evelyne Benoit, Rómulo Aráoz, Denis Servent, Alexei Novikov, Jordi Molgó, Armen Zakarian
, Nat. Prod. Rep.
, 2015
, 32
, 411
- Synthesis of macrocyclic shellfish toxins containing spiroimine moieties. Patrick D. O'Connor, Margaret A. Brimble
, Nat. Prod. Rep.
, 2007
, 24
, 869
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6,6-Spiroimine analogs of (−)-gymnodimine A: synthesis and biological evaluation on nicotinic acetylcholine receptors. Leslie Duroure, Thierry Jousseaume, Rómulo Aráoz, Elvina Barré, Pascal Retailleau, Laurent Chabaud, Jordi Molgó, Catherine Guillou
, Org. Biomol. Chem.
, 2011
, 9
, 8112
- Synthesis of the gymnodimine tetrahydrofuran core through a Ueno–Stork radical cyclization. Sylvestre Toumieux, Redouane Beniazza, Valérie Desvergnes, Rómulo Aráoz, Jordi Molgó, Yannick Landais
, Org. Biomol. Chem.
, 2011
, 9
, 3726
- Spiroimine shellfish poisoning (SSP) and the spirolide family of shellfish toxins: Isolation, structure, biological activity and synthesis. Stéphanie M. Guéret, Margaret A. Brimble
, Nat. Prod. Rep.
, 2010
, 27
, 1350
- Polyketide biosynthesis in dinoflagellates: what makes it different?. Ryan M. Van Wagoner, Masayuki Satake, Jeffrey L. C. Wright
, Nat. Prod. Rep.
, 2014
, 31
, 1101
- Marine natural products: Synthetic aspects. Jonathan C. Morris, Andrew J. Phillips
, Nat. Prod. Rep.
, 2011
, 28
, 269
- Stereoselective synthesis of the spirocyclic core of 13-desmethyl spirolide C using an aza-Claisen rearrangement and an exo-selective Diels–Alder cycloaddition. Andrew D. W. Earl, Freda F. Li, Chao Ma, Daniel P. Furkert, Margaret A. Brimble
, Org. Biomol. Chem.
, 2023
, 21
, 1222
- Coinage metals (Cu, Ag and Au) in the synthesis of natural products. K. C. Majumdar, Biswajit Sinha
, RSC Adv.
, 2014
, 4
, 8085
- Biogenetically inspired syntheses of alkaloid natural products. Justin Kim, Mohammad Movassaghi
, Chem. Soc. Rev.
, 2009
, 38
, 3035