Synthesis of the C1–C26 Northern Portion of Azaspiracid‐1: Kinetic versus Thermodynamic Control of the Formation of the Bis‐spiroketal | Synapse

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Studies Directed toward the Total Synthesis of Azaspiracid: Stereoselective Construction of C1−C12, C13−C19, and C21−C25 FragmentsOriginal Research · 2000 · 70 citations
2Synthetic Studies toward the C5−C20 Domain of the AzaspiracidsOriginal Research · 2001 · 50 citations
3Synthesis of the FGHI Ring System of AzaspiracidOriginal Research · 2001 · 65 citations
4Synthesis 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
5Synthesis of the ABCD Ring System of AzaspiracidOriginal Research · 2001 · 16 citations

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