| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224024 | Tetrahedron | 2010 | 7 Pages |
Abstract
A remarkable stability of anionic species generated from cyclopropene-3-carboxamides toward ring-opening is demonstrated. The resulting cyclopropenyllithium species can be reacted with a range of electrophiles, which allows for efficient introduction of additional substituents at C1 of the strained ring.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ryan Kim, William M. Sherrill, Michael Rubin,