Stereoselective Synthesis of Enantiopure γ-Aminoalcohols by Reduction of Chiral β-Enaminoketones.
✍ Scribed by Cristina Cimarelli; Sandra Giuli; Gianni Palmieri
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 21 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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Stereoselective Synthesis of Chiral γ-Hydroxy-β-methyl Methylcarbinols. -The reaction proceeds in three steps: regioselective hydroboration, oxidation, and reduction to the final products. The protocol can find useful applications in the synthesis of natural products. -
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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 “Full Text” option. The original article is trackable v