Diastereoselective Protonation of Chiral Enolate with Chiral Imides. -Protonation of the lithium enolate (I) of (-)-menthone by chiral imides such as the (R)-imide of conditions (A) generates mainly the cis ketone (III). The selectivity of this process can be completely reversed by using the corres
ChemInform Abstract: Diastereoselective Protonation of Enolates of Chiral Schiff Bases.
β Scribed by M. TABCHEH; C. GUIBOURDENCHE; L. PAPPALARDO; M.-L. ROUMESTANT; P. VIALLEFONT
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 27 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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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
## 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