Response toHeterocyclic tautomerism: reassignment of two crystal structures of 2-amino-1,3-thiazolidin-4-one derivativesby Gzellaet al.(2014)-Reference-Cited by-同舟云学术

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Response toHeterocyclic tautomerism: reassignment of two crystal structures of 2-amino-1,3-thiazolidin-4-one derivativesby Gzellaet al.(2014)

Published:2014-07-31 Issue:8 Volume:70 Page:833-833
ISSN:2053-2296
Container-title:Acta Crystallographica Section C Structural Chemistry
language:
Short-container-title:Acta Crystallogr C

Author:

Váňa Jiří,Hanusek Jiří,Růžička Aleš,Sedlák Miloš

Publisher

International Union of Crystallography (IUCr)

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry,Condensed Matter Physics

Link

http://journals.iucr.org/c/issues/2014/08/00/wq9065/wq9065.pdf

Reference9 articles.

1. 2-Aminothiazoline-4-one and 2-Iminothiazolidine-4-one Derivatives. Part II. Tautomerism.

2. 15N NMR and crystal structure studies of 5-(2-pyridylmethylene)pseudothiohydantoin;† dipolar dephasing experiments for establishing the preferred tautomer in the solid and solution states

3. Heterocyclic tautomerism: reassignment of two crystal structures of 2-amino-1,3-thiazolidin-4-one derivatives

4. Ring Transformation of the S-(2-Oxo-2,3-dihydro-1-benzofuran-3-yl)isothiuronium Bromides to 5-(2-Hydroxyphenyl)-2-imino-1,3-thiazolidin-4-ones

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