Stereoselective hydrogenation of (R)-(+)-pulegone and (2S,5R)-(−)-menthone in presence of β-cyclodextrin and its derivatives
✍ Scribed by Palaniswami Ravi; Ramaswamy Ravichandran; Soundar Divakar
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 311 KB
- Volume
- 148
- Category
- Article
- ISSN
- 1381-1169
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Regio-and stereo-selective reduction of the double bonds in conjugated ketones with numerous reducing agents under various conditions have been studied'. The reactions usually afford mixtures of products, the compositions of which depend on the reagent, the catalyst, the solvent, the pH of the mediu
Highly diastereoselective nucleophilic addition reactions of organometallic reagents to formyl[2.2]paracyclophane derivatives which were ortho-substituted by hydroxy-, alkoxy-and trimethylsilyloxy-groups are reported. The absolute configuration of the newly formed secondary alcohols is assigned on t