Catalytic asymmetric hydrosilylation of butadiynes: A new synthesis of optically active allenes
โ Scribed by Annegret Tillack; Dirk Michalik; Cornelia Koy; Manfred Michalik
- Book ID
- 104262185
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 120 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The Rh-catalyzed hydrosilylation of butadiynes to chiral allenes in the presence of chiral phosphine ligands is d~scribed. For the first time an enantiomeric excess of 22% was achieved using PPM ligand ((2S,4S)-(-)-4-(diphenylphosphino)-2-(diphenylphosphinomethyl)-pyrrolidine).
๐ SIMILAR VOLUMES
Asymmetric hydrosilylation of l-arylbutadienes with trichlorosilane in the presence of a chiral ferrocenylphosphine-palladium catalyst gave optically active allylsilanes, (z)-laryl-1-silyl-Z-butenes and their regioisomers.
B-Amino acids2) are of great current interest because of their naturally occurring as the component of biologically active peptide antibiotics and also their structual relationship to the B-lactam, one of the most biologically important functional groups. We wish to describe here the catalytic asym