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DOI: 10.1055/a-2356-8408
Synthesis and Reactions of Pentacycloundecane Derivatives Related to Cookson’s Dione
M.S. thanks the University Grants Commission (UGC), New Delhi, for the award of a research fellowship.
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Abstract
In this study, a pentacyclic keto-olefin was treated with thallium(III) nitrate trihydrate, resulting in the formation of mono ring-expanded product. However, when the corresponding dialkene was treated with thallium(III) nitrate trihydrate, an unexpected ring-closure product was obtained instead of the expected double ring-expanded product. The use of the Tebbe reagent facilitated the olefination of hindered and enolizable cage dione derivatives, converting both keto moieties into methylene groups and forming the desired diolefin. Notably, conventional Wittig reagents proved to be ineffective in the olefination sequence with cage diones.
Key words
Diels–Alder reaction - photocycloaddition - pentacycloundecanes - Peterson reaction - thallium trinitrate - ring expansionSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2356-8408.
- Supporting Information
Publikationsverlauf
Eingereicht: 25. Mai 2024
Angenommen nach Revision: 12. Juni 2024
Accepted Manuscript online:
28. Juni 2024
Artikel online veröffentlicht:
17. Juli 2024
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- 52 Diolefination of Cage Diones with the Tebbe Reagent; General Procedure The Tebbe reagent (4 equiv) was added dropwise to a precooled solution of the appropriate cage diol (0.78–1.14 mmol) in dry THF at 0 ℃ under N2, and the mixture was stirred at r.t. for 2 h. When the reaction was complete (TLC), 5% aq NaHCO3 was added and the mixture was extracted with EtOAc. The organic layer was washed with brine (20 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, 1% EtOAc–PE). 17 Prepared according to the general procedure from cage diol 16 (200 mg, 1.14 mmol) to give a colorless liquid; yield: 148 mg (74%). IR (CH2Cl2): 2980, 2882, 1740, 1668 cm–1. 1H NMR (400 MHz, CDCl3): δ = 1.60 (d, J = 10.9 Hz, 2 H), 2.19 (s, 4 H), 2.26 (d, J = 12.9 Hz, 2 H), 2.37 (s, 2 H), 2.63 (s, 2 H), 4.70 (s, 2 H), 4.84 (s, 2 H). 13C NMR (100.6 MHz, CDCl3): δ = 155.34, 106.17, 54.46, 48.88, 42.11, 33.74, 32.49. HRMS (ESI): m/z [M + H]+ calcd for C13H15: 171.1166; found: 171.1167.