A family of synthetic receptors has been prepared containing a barbiturate binding site and an appended thiol nucleophile. These are shown to cause large accelerations in the thiolysis reactions of barbiturate active ester derivatives. The size of the acceleration is shown to depend critically on the length and flexibility of the spacer that links the thiol to the receptor.
|Original language||English (US)|
|Number of pages||14|
|State||Published - Jan 9 1995|
ASJC Scopus subject areas
- Drug Discovery
- Organic Chemistry