Sulfamide instead of urea in Biginelli reaction: from black box to reality-Reference-Cited by-同舟云学术

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Sulfamide instead of urea in Biginelli reaction: from black box to reality

Published:2024 Issue:8 Volume:11 Page:2155-2160
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Lyapunov Alexander Yu.¹²,Tarnovskiy Andriy V.¹²,Boron Sergey Yu.¹,Rusanov Eduard B.³,Grabchuk Galyna P.²,Volochnyuk Dmytro M.¹²³,Ryabukhin Serhiy V.¹²³^ORCID

Affiliation:

1. Enamine Ltd, 78 Winston Churchill str., 02094 Kyiv, Ukraine

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

3. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 5 Akademik Kuhar str., 02660 Kyiv, Ukraine

Abstract

The scope and limitations of the classical Biginelli reaction have been expanded to principally novel substrates: sulfamide and its monosubstituted analogues.

Funder

Ministry of Education and Science of Ukraine

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01926H

Reference30 articles.

1. ISOMORPHISM, ISOSTERISM AND COVALENCE.

2. H. L.Friedman , Influence of isosteric replacements upon biological activity , National Academy of Science , Washington , 1951 , vol. 206

3. N. A.Meanwell , in Tactics in Contemporary Drug Design , ed. N. A. Meanwell , Springer Berlin Heidelberg , Berlin, Heidelberg , 2015 , pp. 283–381

4. Saturated bioisosteres of benzene: where to go next?

5. Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances

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