| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1327623 | Journal of Organometallic Chemistry | 2009 | 5 Pages |
Abstract
A study concerning the gold(I)-catalyzed transformation of N-(hex-5-enynyl) tert-butyloxycarbamates is described. The mild conditions employed allow the moderately efficient but stereoselective synthesis of a range of bicyclic carbamates following a formal [4+2] cycloaddition process.
Graphical abstractA study concerning the gold(I)-catalyzed transformation of N-(hex-5-enynyl) tert-butyloxycarbamates is described. The mild conditions employed allow the moderately efficient but stereoselective synthesis of a range of bicyclic carbamates following a formal [4+2] cycloaddition process.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
![Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates](/preview/png/1327623.png "First Page Preview: Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates")
Authors
Andrea Buzas, Florin Istrate, Xavier F. Le Goff, Yann Odabachian, Fabien Gagosz,