Facile synthesis of functionalised phenylphosphinic acid derivatives
✍ Scribed by E. Andrew Boyd; Mark E.K. Boyd; Vincent M. Loh Jr.
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 246 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
## Abstract 2,9‐Dimethyl‐1,10‐phenanthroline (neocuproine, **1**) was functionalised selectively in the 5‐position. Silylation of the methyl groups followed by bromination in the 5‐position was carried out to give the bis(__tert__‐butyldimethylsilyl)‐substituted neocuproine **3** and 5‐bromo‐2,9‐di
acetylamino acrylate, giving &per(poly)fluoroalkyl a-amino acid derivatives in good yields. Keywords Per(po1y)fluoroalkyl iodides, a-acetylaminoacrylate, chromic chloride/iron Initiated by CrCls/Fe redox couple, per(po1y)fluoroalkyl iodides added to methyl a-'
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v