Author:
Smith Lars Borch,Hansen Poul Erik
Abstract
Abstract
A series of 5-acyl-3-methylrhodanines have been synthesized. The structures of those are described using 1H and 13C NMR, deuterium isotope effects on 13C chemical shifts and DFT calculations. The compounds exist as exocyclic enols with intramolecular hydrogen bonds to the C = ONCH3 oxygen. No signs of enhanced mesoionic character were found.
Subject
Physical and Theoretical Chemistry
Cited by
4 articles.
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