期刊
NEW JOURNAL OF CHEMISTRY
卷 29, 期 8, 页码 1001-1003出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b505316a
关键词
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A transition-state analogue (TSA) for an acetal hydrolysis reaction was found to select and amplify a macrocycle from a dynamic combinatorial library (DCL) of disulfides in water. This host was able to accelerate the reaction by a factor of two; a similar value was progressively reached when the macrocycle was gradually produced in the course of the reaction.
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