| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5230128 | Tetrahedron | 2007 | 12 Pages |
Abstract
Photoinduced electron transfer (PET) reactions from triethylamine (TEA) to ketones have been utilized for a clean and efficient route to bicyclo[3.2.1]octanones. A one-pot conversion of bicyclo[2.2.2]octenones to such molecules has been described. MeOH as well as acetonitrile/LiClO4 combinations have been found to be the most effective solvents for these reactions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of bicyclo[3.2.1]octanones via ketyl radical promoted rearrangements under reductive PET conditions](/preview/png/5230128.png "First Page Preview: Synthesis of bicyclo[3.2.1]octanones via ketyl radical promoted rearrangements under reductive PET conditions")
Authors
Somnath Yadav, Srirupa Banerjee, Dwijendralal Maji, Saswati Lahiri,