| Literature DB >> 3616626 |
A D Napper, S J Benkovic, A Tramontano, R A Lerner.
Abstract
A monoclonal antibody elicited by a transition-state analog that is representative of an intramolecular six-membered ring cyclization reaction acted as a stereospecific, enzyme-like catalyst for the appropriate substrate. Formation of a single enantiomer of a delta-lactone from the corresponding racemic delta-hydroxyester was accelerated by the antibody by about a factor of 170, which permitted isolation of the lactone in an enantiomeric excess of about 94 percent. This finding demonstrates the feasibility of catalytic-antibody generation for chemical transformations that require stereochemical control.Entities:
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Year: 1987 PMID: 3616626 DOI: 10.1126/science.3616626
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728