Journal
ORGANIC LETTERS
Volume 19, Issue 15, Pages 4034-4037Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01786
Keywords
-
Categories
Funding
- UNSW Canberra postgraduate research student scholarship scheme
Ask authors/readers for more resources
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 c-ydobutanocucurbit[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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available