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Magnesium-Mediated Regioselective Additions of Bromoform to Quinone Methides and Aurone-Derived Azadienes.
- Source :
-
Synthesis . Jan2025, Vol. 57 Issue 1, p71-83. 13p. - Publication Year :
- 2025
-
Abstract
- The magnesium-mediated addition of bromoform to conjugated electron-deficient alkenes and imines, such as para -quinone methides (p -QMs) and aurone-derived azadienes, respectively, is reported here for the first time. While p -QMs undergo exclusive and hitherto unreported 1,6-addition of bromoform to afford benzylic tribromomethylated diarylmethanes, aurone-derived azadienes undergo both 1,2- and 1,4-additions to furnish α- and γ-tribromomethylamines. A mechanism involving the intermediacy of the tribromomethyl radical has been proposed based on control experiments and EPR studies. Representative synthetic transformations have also been carried out. [ABSTRACT FROM AUTHOR]
- Subjects :
- *QUINONE methides
*EINSTEIN-Podolsky-Rosen experiment
*BROMOFORM
*ALKENES
*IMINES
Subjects
Details
- Language :
- English
- ISSN :
- 00397881
- Volume :
- 57
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- Synthesis
- Publication Type :
- Academic Journal
- Accession number :
- 181466281
- Full Text :
- https://doi.org/10.1055/a-2353-1722