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An optimised in situ procedure for the oxazaborolidine catalysed enantioselective reduction of prochiral ketones

โœ Scribed by K.R.K. Prasad; N.N. Joshi


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
263 KB
Volume
7
Category
Article
ISSN
0957-4166

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๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: An Optimized in sit
โœ K. R. K. PRASAD; N. N. JOSHI ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 27 KB ๐Ÿ‘ 2 views

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.

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## 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, please click on HTML or PDF.

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Several conformationally constrained oxazaborolidine catalysts have been evaluated in the reduction of ketone 1. Readily accessible (1R, 2S ) l-amino-2 .tetralol (B-H) derived oxazaborolidine catalyst (6b) proves to be the most effective and practical catalyst in the reduction of bromo-ketone I (96%

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## 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, please click on HTML or PDF.