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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
- Marine natural products: synthetic aspects. Jonathan C. Morris, Andrew J. Phillips
, Nat. Prod. Rep.
, 2010
, 27
, 1186
- Metal-catalyzed enyne cycloisomerization in natural product total synthesis. Ying Hu, Miao Bai, Ying Yang, Qianghui Zhou
, Org. Chem. Front.
, 2017
, 4
, 2256
- Synthesis of macrocyclic shellfish toxins containing spiroimine moieties. Patrick D. O'Connor, Margaret A. Brimble
, Nat. Prod. Rep.
, 2007
, 24
, 869
- Synthesis of the bis-spiroacetal moiety of the shellfish toxins spirolides B and D using an iterative oxidative radical cyclization strategy. Kai Meilert, Margaret A. Brimble
, Org. Biomol. Chem.
, 2006
, 4
, 2184
- Synthesis of the 1,6,8-trioxadispiro[4.1.5.2]tetradec-11-ene ring system present in the spirolide family of shellfish toxins and its conversion into a 1,6,8-trioxadispiro[4.1.5.2]-tetradec-9-en-12-ol via base-induced rearrangement of an epoxide. Margaret A. Brimble, Daniel P. Furkert
, Org. Biomol. Chem.
, 2004
, 2
, 3573
- [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products. Elizabeth A. Ilardi, Craig E. Stivala, Armen Zakarian
, Chem. Soc. Rev.
, 2009
, 38
, 3133
- Stereoconfining macrocyclizations in the total synthesis of natural products. Kuan Zheng, Ran Hong
, Nat. Prod. Rep.
, 2019
, 36
, 1546
- One-step assembling reaction to the pentacyclic acetal
of pinnatoxins. Jun Ishihara, Shingo Tojo, Akio Kamikawa, Akio Murai
, Chem. Commun.
, 2001
, 1392
- A synergistic approach to polycyclics via a strategic utilization of Claisen rearrangement and olefin
metathesis. Sambasivarao Kotha, Nimita G. Krishna, Somnath Halder, Shilpi Misra
, Org. Biomol. Chem.
, 2011
, 9
, 5597