Asymmetric synthesis of arylselenoalcohols by means of the reduction of organoseleno acetophenones by whole fungal cells
✍ Scribed by Leandro H. Andrade; Álvaro T. Omori; André L.M. Porto; João V. Comasseto
- Book ID
- 113803791
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 123 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1381-1177
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Efficient stereoselective synthesis of sphinganine by the asymmetric borane reduction of ctoxoketoxime trityl ethers is described. Both threo and erythro sphinganine could be obtained with high enantioselectivities by using borane-N,N-diethylaniline complex as a reducing agent.
Stereoselective Synthesis of Sphinganine by Means of Modified Asymmetric Borane Reduction. -A modified asymmetric borane reduction of the ester (I) and the related silyl ether (V) are described. Thus, reduction of the ester yields mainly the threo compound, whereas the silyl ether affords the desir