| Literature DB >> 28731716 |
Yi Zhao1, Vijaybabu Mandadapu1, Hasti Iranmanesh2, Jonathon E Beves2, Anthony I Day1.
Abstract
Two new glycoluril diethers have been prepared, bearing strained cyclobutene and cyclobutane rings at the fused junction of the two imidazolidinone rings. The wide angle of the concave face of the cyclobutano derivative enabled the synthesis of cyclobutanocucurbit[5-8]uril, the largest member being the most significant achievement. A limited binding affinity study compared the new substituted family to classical cucurbit[5-8]uril. Surprisingly lower affinities were found, except for cyclobutanocucurbit[6]uril, which was 3.3-fold higher.Entities:
Year: 2017 PMID: 28731716 DOI: 10.1021/acs.orglett.7b01786
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005