Catalytic multi-step domino and one-pot reactions

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Editor: Prof. Svetlana B. Tsogoeva
Friedrich-Alexander-Universität Erlangen-Nürnberg
 
Multi-step domino (cascade) and one-pot reactions are powerful tools to economically and sustainably build up pharmaceutically relevant compounds, natural products, ligand systems and building blocks for materials science.

In particular, catalytic domino reactions and one-pot processes with excellent selectivity and functional group tolerance are of significant interest for industrial and academic research alike. Such processes, using conventional reagents and also visible light, can simplify the synthesis of pharmaceutical ingredients and drugs. In these so-called domino reactions, all of the required reagents, the catalyst and a solvent are simply mixed in one flask, in which multiple reaction steps take place autonomously without the addition of further reactants. This strategy is in contrast to the conventional "stop-and-go" synthetic approach. These efficient and straightforward synthetic methods make the isolation and purification of intermediate products after each reaction step superfluous, thereby drastically reducing the number of work-up and purification steps, which is superior to conventional organic synthesis.

For this thematic issue, contributions on all types of catalytic multi-step domino and one-pot reactions are welcome.
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Catalytic multi-step domino and one-pot reactions

  • Svetlana B. Tsogoeva

Beilstein J. Org. Chem. 2024, 20, 254–256, doi:10.3762/bjoc.20.25

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Published 08 Feb 2024

Computational studies of Brønsted acid-catalyzed transannular cycloadditions of cycloalkenone hydrazones

  • Manuel Pedrón,
  • Jana Sendra,
  • Irene Ginés,
  • Tomás Tejero,
  • Jose L. Vicario and
  • Pedro Merino

Beilstein J. Org. Chem. 2023, 19, 477–486, doi:10.3762/bjoc.19.37

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Published 20 Apr 2023

Transition-metal-catalyzed domino reactions of strained bicyclic alkenes

  • Austin Pounder,
  • Eric Neufeld,
  • Peter Myler and
  • William Tam

Beilstein J. Org. Chem. 2023, 19, 487–540, doi:10.3762/bjoc.19.38

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Review
Published 24 Apr 2023

Enolates ambushed – asymmetric tandem conjugate addition and subsequent enolate trapping with conventional and less traditional electrophiles

  • Péter Kisszékelyi and
  • Radovan Šebesta

Beilstein J. Org. Chem. 2023, 19, 593–634, doi:10.3762/bjoc.19.44

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Published 04 May 2023

Palladium-catalyzed enantioselective three-component synthesis of α-arylglycine derivatives from glyoxylic acid, sulfonamides and aryltrifluoroborates

  • Bastian Jakob,
  • Nico Schneider,
  • Luca Gengenbach and
  • Georg Manolikakes

Beilstein J. Org. Chem. 2023, 19, 719–726, doi:10.3762/bjoc.19.52

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Published 25 May 2023

Asymmetric tandem conjugate addition and reaction with carbocations on acylimidazole Michael acceptors

  • Brigita Mudráková,
  • Renata Marcia de Figueiredo,
  • Jean-Marc Campagne and
  • Radovan Šebesta

Beilstein J. Org. Chem. 2023, 19, 881–888, doi:10.3762/bjoc.19.65

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Published 16 Jun 2023

New one-pot synthesis of 4-arylpyrazolo[3,4-b]pyridin-6-ones based on 5-aminopyrazoles and azlactones

  • Vladislav Yu. Shuvalov,
  • Ekaterina Yu. Vlasova,
  • Tatyana Yu. Zheleznova and
  • Alexander S. Fisyuk

Beilstein J. Org. Chem. 2023, 19, 1155–1160, doi:10.3762/bjoc.19.83

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Published 02 Aug 2023

Unravelling a trichloroacetic acid-catalyzed cascade access to benzo[f]chromeno[2,3-h]quinoxalinoporphyrins

  • Chandra Sekhar Tekuri,
  • Pargat Singh and
  • Mahendra Nath

Beilstein J. Org. Chem. 2023, 19, 1216–1224, doi:10.3762/bjoc.19.89

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Published 11 Aug 2023

Acetaldehyde in the Enders triple cascade reaction via acetaldehyde dimethyl acetal

  • Alessandro Brusa,
  • Debora Iapadre,
  • Maria Edith Casacchia,
  • Alessio Carioscia,
  • Giuliana Giorgianni,
  • Giandomenico Magagnano,
  • Fabio Pesciaioli and
  • Armando Carlone

Beilstein J. Org. Chem. 2023, 19, 1243–1250, doi:10.3762/bjoc.19.92

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Published 24 Aug 2023

Consecutive four-component synthesis of trisubstituted 3-iodoindoles by an alkynylation–cyclization–iodination–alkylation sequence

  • Nadia Ledermann,
  • Alae-Eddine Moubsit and
  • Thomas J. J. Müller

Beilstein J. Org. Chem. 2023, 19, 1379–1385, doi:10.3762/bjoc.19.99

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Published 14 Sep 2023

One-pot nucleophilic substitution–double click reactions of biazides leading to functionalized bis(1,2,3-triazole) derivatives

  • Hans-Ulrich Reissig and
  • Fei Yu

Beilstein J. Org. Chem. 2023, 19, 1399–1407, doi:10.3762/bjoc.19.101

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Published 18 Sep 2023

Decarboxylative 1,3-dipolar cycloaddition of amino acids for the synthesis of heterocyclic compounds

  • Xiaofeng Zhang,
  • Xiaoming Ma and
  • Wei Zhang

Beilstein J. Org. Chem. 2023, 19, 1677–1693, doi:10.3762/bjoc.19.123

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Published 06 Nov 2023
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