The radical polymerization of N-tert-butyl-N-allylacrylamide (t-BAA) was carried out in a dimethyl sulfoxide/H 2 O mixture in the presence of β€-cyclodextrin (β€-CD). The polymerization proceeded with the complete cyclization of the t-BAA unit and yielded optically active poly(t-BAA). The IR spectrum
Asymmetric hydrosilylation of prochiral ketones in the presence of N-benzyl-N-methylephedrinium halometallates
β Scribed by K I Rubina; Yu Sh Goldberg; M V Shymanska; E Lukevics
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 420 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0268-2605
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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.