| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223296 | Tetrahedron | 2010 | 6 Pages |
Abstract
A skeletal carbenoid rearrangement of the gem-bromochlorospiropentanes in the presence of methyllithium has been studied. The synthetic and mechanistic aspects of this rearrangement as well as the influence of the halogen atom nature on the reaction pathway are discussed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kseniya N. Sedenkova, Elena B. Averina, Yuri K. Grishin, Tamara S. Kuznetzova, Nikolai S. Zefirov,