Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 1: Construction of the Enantiomerically Pure C1–C20, C21–C27, and C28–C40 Fragments | Synapse

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1Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, <i>Mytilus edulis</i>Original Research · 1998 · 408 citations
2Studies Directed toward the Total Synthesis of Azaspiracid: Stereoselective Construction of C1−C12, C13−C19, and C21−C25 FragmentsOriginal Research · 2000 · 71 citations
3Synthesis of the (+)-C26–C40 Domain of the Azaspiracids by a Novel Double Intramolecular Hetero-Michael Addition Strategy This work was supported by the United States National Institute of Environmental Health Sciences (NIEHS; grant number ES10615), NIH, and by Bristol-Myers Squibb (CJF). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIEHS, NIH, or BMS. We thank Dr. A. B. Dounay and Dr. G. Florence for critical reading of the manuscript.Original Research · 2001 · 76 citations
4Synthetic Studies toward the C5−C20 Domain of the AzaspiracidsOriginal Research · 2001 · 50 citations
5Palladium-catalyzed coupling of allylic acetates with aryl- and vinylstannanesOriginal Research · 1990 · 161 citations

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