Abstract
Radicalic bromination of1,2, and3 leads to products with halogen in the isopropyl group. The corresponding olefins are obtained by elimination of HBr.
Zusammenfassung
Die radikalische Bromierung von1,2 und3 führt zu in der Seitenkette halogenierten Produkten. Eliminierung von HBr liefert die entsprechenden Olefine.
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Haslinger, E., Kalchhauser, H. & Steindl, H. Bromination of resin acid derivatives. Monatsh Chem 114, 1259–1265 (1983). https://doi.org/10.1007/BF00799941
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DOI: https://doi.org/10.1007/BF00799941
Keywords
- 17,19-Dinoratis-15-ene-4,13,14-tricarboxylic acid, 16-(1-methylethyl), cyclic-13,14-anhydride (4α,8α,12α) and derivatives
- 17,19-Dinoratis-15-ene-4,13,14-tricarboxylic acid, 16-(1-methylethyl), 4,13,14-trimethylester (4α,8α,12α,13β,14α) and derivatives
- 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1α,4aα,4bβ,10aα)] and derivatives