Asymmetric Synthesis of β-Hydroxy Esters Having Three Consecutive Chiral Centers with a Reductase from Bakers' Yeast. -The title reaction is investigated with β-keto esters (I) having a secondary alkyl group at the α-position. The corresponding β-hydroxy esters can be isolated in excellent enantios
ChemInform Abstract: β-Hydroxypiperidinecarboxylates: Additions to the Chiral Pool from Bakers′ Yeast Reductions of β-Ketopiperidinecarboxylates.
✍ Scribed by David W. Knight; Neil Lewis; Andrew C. Share; David Haigh
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 30
- 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 “Full Text” 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 “Full Text” 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 “Full Text” option. The original article is trackable v