Conformational preferences in some aryl substituted heterocyclic compounds exhibiting restricted internal rotation about C–N bonds
- 1 January 1974
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 6,p. 225-226
- https://doi.org/10.1039/c39740000225
Abstract
X-Ray studies of the thermodynamically less stable (in solution) diastereoisomeric rotational isomer of 3-(2-bromophenyl)-5-methyl-2-thiohydantion (II) show that the bromine atom is transoid to the 5-methyl group.Keywords
This publication has 0 references indexed in Scilit: