Journal
ORGANIC LETTERS
Volume 4, Issue 2, Pages 217-220Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol017117s
Keywords
-
Categories
Ask authors/readers for more resources
[GRAPHICS] A combination of NMR, IR, and ab initio techniques reveals the striking structural similarities of an exemplary H-bonded complex of an N-acyloxazolidinone with an N,N'-disubstituted electron-poor thiourea and the corresponding Lewis acid complex. Although the H-bond association constant is lower than for the Lewis acid adduct, Diels-Alder reactions are accelerated and stereochemically altered in a fashion similar to weak Lewis acids.
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