Increasing chiral recognition in acetal formation
Copyright policy )Increasing chiral recognition in acetal formation
AbstractThe 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.
- TU Wien Austria
- University of Vienna Austria
Pharmacology, Models, Molecular, Pharmakologie, Sulfonamides, Molecular Structure, Chemistry, Organic, Molecular Conformation, Stereoisomerism, Toxicology, Ligands, Chemistry, Lactones, Acetals, Glucose, Models, Chemical, Toxikologie, 3012 Pharmacy, 3012 Pharmazie
Pharmacology, Models, Molecular, Pharmakologie, Sulfonamides, Molecular Structure, Chemistry, Organic, Molecular Conformation, Stereoisomerism, Toxicology, Ligands, Chemistry, Lactones, Acetals, Glucose, Models, Chemical, Toxikologie, 3012 Pharmacy, 3012 Pharmazie
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