ChemInform Abstract: Synthesis of 2-Amino-2′-diphenylphosphino-1,1′-binaphthyl (MAP) and Its Accelerating Effect on the Pd(0)-Catalyzed N-Arylation.
✍ Scribed by Stepan Vyskocil; Martin Smrcina; Pavel Kocovsky
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Synthesis of 2-Amino-2'-diphenylphosphino-1,1'-binaphthyl (MAP) and Its Accelerating Effect on the Pd(0)-Catalyzed N-Arylation.
-The title compound (R)-(I), available from (R)-(II) in four steps, is found to exhibit an accelerating effect on the Pd-catalyzed Hartwig-Buchwald N-phenylation of racemic (II) and related compounds. However, no kinetic resolution is observed.
📜 SIMILAR VOLUMES
Derivatives of 2-Amino-2'-diphenylphosphino-1,1'-binaphthyl (MAP) and Their Application in Asymmetric Palladium(0)-Catalyzed Allylic Substitution. -The novel chiral biaryls (I), readily synthesized from the corresponding N-unsubstituted optically active precursor, are utilized as chiral ligands in
Direct Palladium-Catalyzed Phosphinylation of Aryl Triflates with Secondary Phosphines. Its Scope and Limitations: The Synthesis of Optically Active Carboxylated 2-(Diphenylphosphino)-1,1'binaphthalenes. -Treatment of aryl triflates with secondary phosphines in the presence of PdCl 2 (PPh 3 ) 2 is