| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229237 | Tetrahedron | 2007 | 8 Pages |
Abstract
The electrohydrocyclization of tethered enone/enoate or bisenone systems which contain an alkoxyl substituent in the tether was studied. Rather surprisingly, the cyclization of these compounds afforded very different products depending upon the alkoxy substituent. This behavior and its potential applications will be discussed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Renuka Manchanayakage, Duncan Omune, Christopher Hayes, Scott T. Handy,