ChemInform Abstract: Novel Electronic Effects of Remote Substituents on the Oxazaborolidine- Catalyzed Enantioselective Reduction of Ketones.
β Scribed by E. J. COREY; C. J. HELAL
- Book ID
- 112029800
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
## Abstract The chiral amine synthesized from Lβvaline methyl ester and 5βchloro salicylaldehyde proves as good catalyst for the enantioselective oxazaborolidine reduction of prochiral ketones.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
An Optimized in situ Procedure for the Oxazaborolidine Catalyzed Enantioselective Reduction of Prochiral Ketones. -The catalyst prepared from (S)-diphenyl prolinol is found to be the best amongst several other analogues for the reduction of alkyl aryl ketones. -(PRASAD, K. R.