## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis of Azobenzenes from Quinone Acetals and Arylhydrazines.
β Scribed by M. Carmen Carreno; Gerardo Fernandez Mudarra; Estibaliz Merino; Maria Ribagorda
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 165 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
In the absence of any added acidic catalyst quinone acetals as well as simple ketone and aldehyde acetals react with a variety of substituted anilines to form imines [Eq. (a)]. Contrary to what is expected from arguments based on their nucleophilicity, the most reactive anilines are those bearing el
A convergent enantioselective synthesis of ()-royleanone (1) is described starting from enantiomerically pure (S)-3-hydroxy-2-isopropyl-5-tert-butylsulfinyl-p-benzoquinone, which is readily available from 3-isopropyl-1,2,4-trimethoxybenzene and 1,3,3-trimethyl-2-vinylcyclohexene. The key step is a t