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Ring-closure reactions of functionalized vinyl sulfonamides (microreview)

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Chemistry of Heterocyclic Compounds Aims and scope

Diversity-oriented synthesis embodied in a strategy of pairing vinyl sulfonamide moiety with other functional groups resulted in an array of skeletally diverse 5–8-membered sultams (cyclic sulfonamides) in the fewest possible steps. In particular, this strategy allows utilization of a number of cyclization protocols including intramolecular Michael, Diels–Alder, Heck, Pauson–Khand, Baylis–Hillman reactions, ring-closing metathesis (RCM) and others.

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Authors and Affiliations

  1. Enamine Ltd., 78 Chervonotkatska St., Kyiv, 02094, Ukraine

    Alexey V. Dodrydnev & Taras V. Omelian

  2. Taras Shevchenko National University of Kyiv, 60 Volodymyrska St., Kyiv, 01601, Ukraine

    Alexey V. Dodrydnev & Taras V. Omelian

Authors
  1. Alexey V. Dodrydnev
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  2. Taras V. Omelian
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Correspondence to Alexey V. Dodrydnev.

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Dedicated to Prof. Yulian M. Volovenko on the occasion of his 71st birthday

Published in Khimiya Geterotsiklicheskikh Soedinenii, 2021, 57(6), 630–632

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Dodrydnev, A.V., Omelian, T.V. Ring-closure reactions of functionalized vinyl sulfonamides (microreview). Chem Heterocycl Comp 57, 630–632 (2021). https://doi.org/10.1007/s10593-021-02960-0

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  • DOI: https://doi.org/10.1007/s10593-021-02960-0

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