| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264039 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
- New phosphonylation reagents were developed.
- Benzotriazole surrogates showing higher stabilities than the chlorophosphates.
- The 1H-benzo[d][1,2,3]triazol-1-yl-1-phosphonates were obtained in high yields.
- Efficient phosphonylation of N-, O-, and S-nucleophiles in good yields.
- Establish the structure of a conjugate by a single crystal X-ray structure study.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Deepak S. Panmand, Anand D. Tiwari, Siva S. Panda, Jean-Christophe M. Monbaliu, Lucas K. Beagle, Abdullah M. Asiri, Christian V. Stevens, Peter J. Steel, C. Dennis Hall, Alan R. Katritzky,