Publication | Closed Access
Biomimetic Dehydrogenative Diels–Alder Cycloadditions: Total Syntheses of Brosimones A and B
64
Citations
40
References
2013
Year
Bioorganic ChemistryEngineeringBiochemistryAlkene MetathesisNatural SciencesSilver NanoparticlesBrosimones AOrganic ChemistryNatural ProductsSynthetic ChemistryChemistryTotal SynthesesOnline DeliveryBiomolecular EngineeringNatural Product Synthesis
Passing (H2) gas: Concise syntheses of the natural products brosimones A and B have been achieved using sequential dehydrogenative Diels–Alder (DHDA) cycloadditions. The syntheses employ either Pt/C-cyclopentene or DDQ to effect dehydrogenation of prenylchalcone substrates in combination with silver nanoparticles to promote subsequent Diels–Alder cycloadditions. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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