Synthesis and structural investigation of new isothiochromen-4-one 2,2-dioxide derivatives View Full Text


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Article Info

DATE

2016-02

AUTHORS

Olena O. Shyshkina, Volodymyr V. Medviediev, Yulian M. Volovenko, Oleg V. Shishkin

ABSTRACT

This article presents a combined experimental and computational study of novel isothiochromene 2,2-dioxide derivatives, which were synthesized by the electrophilic substitution reactions. The compounds have been studied by NMR, IR spectroscopy and single-crystal X-ray analysis. According to X-ray diffraction data, the six-membered ring of 6 adopts a distorted half-chair conformation, but in case of compounds 7 and 8, we have a twist-boat conformation of the six-membered ring with deviation of the S1 and C8 atoms from the mean plane of the remaining atoms of the ring, respectively. Results of quantum-chemical calculations of possible isomers and tautomers of the isolated oxime 8 and azo compounds 10 at the B3LYP/aug-cc-pVDZ level indicate that the oxime-oxo tautomer (8a) is more stable than the nitroso-hydroxy tautomer (8b) in agreement with the crystal data and that the keto tautomer (II) is more stable than the hydroxyl tautomer (I) and zwitterion tautomer (III), because of a strong intramolecular hydrogen bond N–H···O. More... »

PAGES

273-280

References to SciGraph publications

  • 2013-02. Novel transformations of 1H-isothiochromen-4(3H)-one 2,2-dioxide in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
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    http://scigraph.springernature.com/pub.10.1007/s11224-015-0723-4

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    http://dx.doi.org/10.1007/s11224-015-0723-4

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