| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223261 | Tetrahedron | 2009 | 5 Pages |
Abstract
The reaction of stabilized allylic-type carbocations with electron rich olefins was investigated. In most cases a facile cyclobutane ring formation was observed by [2+2] cycloaddition reaction promoted by Brønsted or Lewis acids. Some attempts were made to investigate the mechanistic pathway. After de-racemization the chiral cyclobutane containing diols were obtained as a potential chiral platform for new ligands.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Renata Siedlecka,