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Thiazolidine-2,4-dithione in the Knoevenagel/Hetero Diels–Alder Domino Reaction

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Abstract

Thiazolidine-2,4-dithione reacts with 2-allyloxybenzaldehyde derivatives to form 3,5a,6,11b-tetrahydro-2H,5H-chromeno[4',3':4,5]thiopyrano[2,3-d][1,3]thiazole-2-thiones. The reaction involves an exo-transition state.

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Authors and Affiliations

  1. Ivan Franko National University of Lviv, 79005, Lviv, Ukraine

    Y. V. Ostapiuk & V. S. Matiychuk

  2. Danylo Halytsky Lviv National Medical University, 79010, Lviv, Ukraine

    T. I. Chaban

Authors
  1. Y. V. Ostapiuk
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  2. T. I. Chaban
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  3. V. S. Matiychuk
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Correspondence to V. S. Matiychuk.

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Ostapiuk, Y.V., Chaban, T.I. & Matiychuk, V.S. Thiazolidine-2,4-dithione in the Knoevenagel/Hetero Diels–Alder Domino Reaction. Russ J Org Chem 56, 1495–1497 (2020). https://doi.org/10.1134/S1070428020080242

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  • DOI: https://doi.org/10.1134/S1070428020080242

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