## Abstract A concise and enantioselective synthesis of (__S__)‐ethyl 2‐cyclopentyl‐2‐hydroxy‐2‐arylacetate, a key intermediate for the muscarinic receptor, is reported. The tertiary stereogenic center was constructed with good stereoselectivity through the __L‐__proline‐catalyzed direct asymmetric
ChemInform Abstract: Enantioselective Aldol Reaction of α-Ketoester and Cyclopentanone Catalyzed by L-Proline.
✍ Scribed by Jiming Xiang; Baolin Li
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The catalytic system is excellent for direct aldol reactions of cyclic and acyclic ketones with aromatic and aliphatic aldehydes.
## 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 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