Angewandte Chemie International Edition · 2019 · 63 citations · 40 references
Natural SciencesChemistryBiocatalysisBioorganic ChemistryOrganic ChemistryBiomimetic SynthesisDiversity-oriented SynthesisHeterocyclic ChemistryPhotochemical SynthesisPhotochemistryRetrosynthetic Analysis[2+2] CycloadditionBiomimetic Photochemical SynthesisNatural Product Total SynthesisPhotocyclization ReactionsRing-forming Reactions
The short, efficient total synthesis of (+)-aquatolide was achieved by a biomimetic transannular [2+2] photocycloaddition, and provides the first example of constructing a 5/5/4/8-ring system from asteriscunolides. Furthermore, the reaction leading to a 5/4/4/7-ring system, the originally proposed structure of aquatolide, was also developed. This strategy achieved syntheses of five more humulanolides, (-)-asteriscunolides A, C, D, and I, and (+)-tetradehydroasteriscanolide.
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Total synthesis of the Daphniphyllum alkaloid daphenylline
Zhaoyong Lu, Yong Li, Jun Deng et al. · Nature Chemistry · 2013 · 278 citations
Scott A. Frank, Dustin J. Mergott, William Roush · Journal of the American Chemical Society · 2002 · 230 citations