| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268661 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Solutions of heterocycles having an allyl sulfide unit and simple alkenes in 50% t-BuOH/H2O undergo reversible olefin metathesis reactions with the second generation Hoveyda-Grubbs catalyst. The choice of functional groups is limited by competitive chelation of some heterocycles with the catalyst, and other stereoelectronic effects.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Luke Hunter, Glenn C. Condie, Margaret M. Harding,