Abstract
The concerted mechanism for the new reaction of acylamidation of alkenes and alkynes is proposed on the basis of syn-stereospecifity observed and the study of the reagent structure.
| Original language | English |
|---|---|
| Pages (from-to) | 5577-5584 |
| Number of pages | 8 |
| Journal | Tetrahedron |
| Volume | 47 |
| Issue number | 29 |
| DOIs | |
| Publication status | Published - 1991 Jul 15 |
| Externally published | Yes |
Keywords
- 6-fluoro-5,6-dihydro-1,3-oxazines
- acylamidation
- acylation
- cycloaddition.
- β-amidoketones
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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Cite this
Gridnev, I. D., Shastin, A. V., & Balenkova, E. S. (1991). The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction. Tetrahedron, 47(29), 5577-5584. https://doi.org/10.1016/S0040-4020(01)80989-3