Literature DB >> 16944091

Domino syntheses of bioactive tetronic and tetramic acids.

Rainer Schobert1.   

Abstract

Natural products containing tetronic acid or tetramic acid moieties continue to attract the interest of chemists, biologists, and physicians due to their challenging structures and to the wide range of biological activities they display. This review portrays the structural varieties of tetronic and tetramic acids and the spectrum of possible therapeutically relevant effects in man for exemplary derivatives. Their biosynthetic origin from alpha-amino and alpha-hydroxy acids is briefly discussed as is the relationship between their structures and their modes of interaction with biochemical effectors such as metal cations or enzymes. A short overview of laboratory syntheses of the heterocyclic core structures of tetramic and tetronic acids is provided with an emphasis on those emulating the biosynthesis. A synthesis from the alpha-amino or alpha-hydroxy esters and the cumulated phosphorus ylide Ph(3)PCCO based upon a domino addition-intra-Wittig alkenation sequence is presented with applications to the preparation of the antibiotics reutericyclin and tenuazonic acid, the cytotoxic melophlin B, and the enzyme inhibitor RK-682. Procedural advantages of immobilizing either starting component by attaching it to a resin and its exploitation in the parallel synthesis of libraries of potential drug candidates are described. The basic domino reaction can even be extended by further C-C bond forming steps when starting from suitable alpha-hydroxy or alpha-amino allyl esters. Depending on the chosen reaction conditions, bioactive intermediates of formally three to seven step long cascades can be obtained. Among them, herbicidal 3-alkyltetronic acids and lactone endoperoxides with antiplasmodial activity exceeding that of the natural antimalarial lead artemisinin. Hence, this domino reaction gives access to diversely functionalized derivatives of tetronic and tetramic acids. As it can also be ported to solid phase, it is ideally suited for parallel and combinatorial processing. Future developments might include running such domino sequences in continuous mode in arrays of "labs on microchips".

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Year:  2006        PMID: 16944091     DOI: 10.1007/s00114-006-0152-8

Source DB:  PubMed          Journal:  Naturwissenschaften        ISSN: 0028-1042


  22 in total

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Journal:  Chem Rev       Date:  1996-02-01       Impact factor: 60.622

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Authors:  Rainer Schobert; Carsten Jagusch
Journal:  J Org Chem       Date:  2005-07-22       Impact factor: 4.354

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Authors:  Rainer Schobert; Carsten Jagusch; Claire Melanophy; Gillian Mullen
Journal:  Org Biomol Chem       Date:  2004-11-05       Impact factor: 3.876

9.  Characterization of reutericyclin produced by Lactobacillus reuteri LTH2584.

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Journal:  Appl Environ Microbiol       Date:  2000-10       Impact factor: 4.792

10.  Hydroperoxide and endoperoxide lactones from photooxygenation of 3-alkylidenedihydrofuran-2,4-diones.

Authors:  Rainer Schobert; Ralf Stehle; Wolfgang Milius
Journal:  J Org Chem       Date:  2003-12-12       Impact factor: 4.354

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Review 4.  Marine-derived metabolites of S-adenosylmethionine as templates for new anti-infectives.

Authors:  Janice R Sufrin; Steven Finckbeiner; Colin M Oliver
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5.  Synthesis and Crystal Structure Characterization of Zinc (II) Tetronic Acid Complexes.

Authors:  K C Prousis; G Athanasellis; V Stefanou; D Matiadis; E Kokalari; O Igglessi-Markopoulou; V McKee; J Markopoulos
Journal:  Bioinorg Chem Appl       Date:  2010-11-04       Impact factor: 7.778

6.  Asymmetric synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones including facile conversion to tetronic acids: application to (+)-maculalactone A.

Authors:  Richard J Duffy; Kay A Morris; Ravikrishna Vallakati; Wei Zhang; Daniel Romo
Journal:  J Org Chem       Date:  2009-07-03       Impact factor: 4.354

7.  Total synthesis and biological evaluation of the tetramic acid based natural product harzianic acid and its stereoisomers.

Authors:  Alan R Healy; Francesco Vinale; Matteo Lorito; Nicholas J Westwood
Journal:  Org Lett       Date:  2015-01-28       Impact factor: 6.005

8.  Stereochemical Assignment of the Protein-Protein Interaction Inhibitor JBIR-22 by Total Synthesis.

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Journal:  Angew Chem Weinheim Bergstr Ger       Date:  2015-02-04

9.  (S)-Reutericyclin: Susceptibility Testing and In Vivo Effect on Murine Fecal Microbiome and Volatile Organic Compounds.

Authors:  Bernhard Kienesberger; Beate Obermüller; Georg Singer; Barbara Mittl; Reingard Grabherr; Sigrid Mayrhofer; Stefan Heinl; Vanessa Stadlbauer; Angela Horvath; Wolfram Miekisch; Patricia Fuchs; Ingeborg Klymiuk; Holger Till; Christoph Castellani
Journal:  Int J Mol Sci       Date:  2021-06-15       Impact factor: 5.923

10.  Synthesis of a leopolic acid-inspired tetramic acid with antimicrobial activity against multidrug-resistant bacteria.

Authors:  Luce Mattio; Loana Musso; Leonardo Scaglioni; Andrea Pinto; Piera Anna Martino; Sabrina Dallavalle
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