Advances in Bifunctional Organocatalysis

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Catalysis in Organic and Polymer Chemistry".

Deadline for manuscript submissions: closed (10 October 2021) | Viewed by 417

Special Issue Editor


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Guest Editor
Organic Chemistry Department, Módulo 1, Lab. 503, Faculty of Science, Universidad Autónoma de Madrid C/Francisco Tomás y Valiente, 728049 Madrid, Spain
Interests: organocatalysis; bifunctional; asymmetric synthesis; hydrogen-bond; enantioselective; thiourea; squaramide; cinchona alkaloid

Special Issue Information

Dear Colleagues,

Since the initial introduction of organocatalysis, defined in 2000 as the use of molecules of low molecular weight to perform organic reactions, it has become an important alternative to asymmetric synthesis. Its power as a synthetic tool is emphasized by the large number of new reactions and activation modes described in the literature during the last couple of decades. Nowadays, organocatalysis represents an important option since it also presents the possibility of carrying out cascade reactions, allowing the construction of enantiopure, sophisticated targets in a single operation with the use of a single catalyst; it also represents a key step in the synthesis of intermediates of different natural products and biologically active compounds. The use of catalysts based on non-covalent interactions has been explored as an alternative methodology for the catalytic activation of a wide variety of substrates with different natures. Among them, bifunctional catalysts that can promote enantioselective processes through hydrogen-bonding have been widely explored in recent decades. These catalysts, based on a hydrogen bond donor core (mainly thiourea or squaramide) decorated with a second functionality, allow the synergistic activation of both coupling partners involved in the reaction, giving access to products that are otherwise difficult to synthesize. The secondary functionality has been particularly modified in recent years in order to develop new organocatalysts able to activate substrates of different natures. Therefore, recently, bifunctional organocatalysts have been widely employed in the literature, making this family of catalysts a powerful tool in asymmetric synthesis, with further potential yet to be exploited.

Dr. Jose A. Fernandez-Salas
Guest Editor

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Keywords

  • Organocatalysis
  • bifunctional
  • asymmetric synthesis
  • hydrogen-bond
  • enantioselective
  • thiourea
  • squaramide
  • cinchona alkaloid

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