Synthesis of novel ferrocenylphosphine–amidine ligands and their application in Pd-catalyzed asymmetric allylic alkylation
✍ Scribed by Xiangping Hu; Huilin Chen; Xinquan Hu; Huicong Dai; Changmin Bai; Junwei Wang; Zhuo Zheng
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 189 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A family of novel ferrocenylphosphine-amidine ligands derived from (R)-(S)-PPFNH 2 -R 5 was applied to the palladium-catalyzed asymmetric allylic alkylation of 1,3-diphenylprop-2-en-1-yl acetate 8a or pivalate 8b with dimethyl malonate. Up to 94% e.e. was achieved when ligand 6b was used.
📜 SIMILAR VOLUMES
Some novel ferrocenylphosphine-amidine ligands with central and planar chirality were prepared from (R,S p )-PPFNH 2 -R 3 and its diastereomer (S,S p )-PPFNH 2 3a. The efficiency and diastereomeric impact of these ferrocenylphosphine-amidine ligands in the palladium-catalyzed asymmetric allylic subs
An efficient and flexible asymmetric synthesis of planar chiral ferrocenyl ligands bearing a stereogenic centre at the β-position to the metallocene backbone is described. A variety of donor groups can be independently introduced as electrophiles, thus allowing electronic and steric fine-tuning of t