Synthesis of 4-(2-diphenylphosphino-1-naphthyl)-2-phenylquinazoline; a potential PN chelating ligand for asymmetric catalysis
✍ Scribed by V Gautheron Chapoulaud; J Audoux; N Plé; A Turck; G Quéguiner
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 168 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
We describe a multistep synthesis leading in a good yield to the title compound. The biaryl linkage was formed in a Pd-catalysed coupling of 2-phenyl-4-chloroquinazoline with 2-methoxy-l-naphthylboronic acid. A further metal-catalysed reaction gave the formation of the naphthylphosphorus bond allowing us to obtain the required phosphonimine ligand 1 as the racemate.
📜 SIMILAR VOLUMES
## Abstract The radiochemical synthesis of the high affinity, selective sigma receptor ligand, N^1^‐3‐[^18^F]Fluoropropyl‐N^4^‐2‐([3,4‐dichlorophenyl]ethyl)piperazine, is reported. The labeled compound is prepared by fluoride displacement on a bismethanesulfonate salt of the propyl methanesulfonylo