期刊
ORGANIC CHEMISTRY FRONTIERS
卷 1, 期 6, 页码 661-673出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4qo00123k
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资金
- EPSRC [EP/E055273/1]
- German Academic Exchange Service (DAAD)
- A*STAR for a National Science Scholarship
- EPSRC [EP/E055273/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/E055273/1] Funding Source: researchfish
The palladium-catalyzed cascade cyclization of silylated bromoenynes and alkenylstannanes provides a straightforward route to a range of bicyclic silylated cyclohexadienes. Mechanistic insights into aspects of carbopalladation and unusual palladium-mediated isomerizations have been obtained through the detection of reaction intermediates, the isolation of byproducts, and reaction monitoring by VT NMR spectroscopy. The utility of the bicyclic products is illustrated through oxidation to bicyclic enones and phenols.
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