Diastereoselective hydrogenations of unsymmetrically substituted aromatics
✍ Scribed by Christina Exl; Eva Ferstl; Dr. Helmut Hönig; Renate Rogi-Kohlenprath
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 635 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A series of new unsymmetrically substituted subphthalocyanines containing iodo or octylthioether substituents on the outer aromatic rings have been synthesized. The statistical reaction of one equivalent of 1,2-dicyano-3-iodobenzene whether with two equivalents of 1,2-dicyano-4-octylthiobenzene or w
## Abstract For Abstract see ChemInform Abstract in Full Text.
The reactivity of tert-butoxy radicals with methyl substituted aromatic compounds is almost exclusively determined by the aromatic moiety and almost independent of the methyl group position. The hydrogen abstraction from the carbon (Y to the aromatic ring is hardly sensitive to the produced radical