Increasing chiral recognition in acetal formation
✍ Scribed by Christian R. Noe; Max Knollmüller; Edith Jangg; Günter P. Gmeiner; Ernst Urban; Simon Eppacher
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 183 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The design of substituted lactols is described, which in their reaction with racemic alkyl aryl carbinols react preferentially with one of the enantiomers exhibiting selectivities up to 14:1. Chirality, 2009. © 2008 Wiley‐Liss, Inc.
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