A simple route to chiral ferrocenyl alcohols
β Scribed by J. Wright; L. Frambes; P. Reeves
- Book ID
- 103228829
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 317 KB
- Volume
- 476
- Category
- Article
- ISSN
- 0022-328X
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π SIMILAR VOLUMES
Reaction of chlorides of nonsymmetrically substituted phosphinic and phosphinous acid with (-)-l,2:3,5-disubstituted-ct-D-glucofuranose proceeds with very high stereoselectivity to give stereochemically pure phosphinic and phosphinous acid esters, which are starting reagents for preparation of chira
Optically active ferrocenyl amino alcohols have been prepared from commercially available L-alaninol, L-leucinol and L-valinol. They have been utilized as chiral ligands in the catalytic addition of diethylzinc to aldehydes. The influence of the substituents on the stereogenic centers of the ligand
## Abstract For Abstract see ChemInform Abstract in Full Text.