Reduction of Plutonium Hexafluoride Using Gaseous Reagents
β Scribed by A. M. Pokidyshev; I. A. Tsarenko; V. F. Serik; V. B. Sokolov
- Book ID
- 111572190
- Publisher
- Springer US
- Year
- 2003
- Tongue
- English
- Weight
- 82 KB
- Volume
- 95
- Category
- Article
- ISSN
- 1573-8205
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π SIMILAR VOLUMES
Some chiral acetals are cleaved by organoaluminum reagents. The products are formed diastereoselectively, and the removal of the chiral auxiliary affords optically active alcohols. A recent communication by Bartlett, Johnson and Elliott1 on the acetal derived from (-)-(2$4\_R)-2,4-pentanediol has pr
## Abstract Under mild reaction conditions, the C=C double bond inisatinβderived electronβdeficient alkenes has been exclusively reduced in the presence of alkylphosphanes and water to afford the corresponding reduction products in good to excellent yields. A plausible mechanism is proposed on the
After a brief review of the literature on asymmetric reduction of prochiral ketones using polymer-supported catalysts or reagents some new results in this field are presented. In particular asymmetric reduction is reported here using (1) chiral oxazaborolidines as catalyst and BH3 as reducing agent,