Literature DB >> 14870853

Combining the use of solid-supported transition metal catalysis with microwave irradiation in solution-phase parallel library synthesis.

Michael G Organ1, Stanislas Mayer, Franck Lepifre, Blaise N'Zemba, Jayantilal Khatri.   

Abstract

Microwave heating methods have been combined with the use of solid-supported catalysts to produce small solution-phase libraries of medicinally-relevant compounds. Palladium supported on charcoal (Pd/C) has been used to produce libraries of pyrazole compounds for screening in COX II studies via Suzuki cross coupling reactions, while the same catalyst has been used also to produce styryl-based nAChR compounds using analogous chemistry. Although the reaction substrates are very different (aryl vs. vinyl), this catalyst system provided consistently good and reliable results. The use of a polystyrene-supported Ru catalyst for ring-closing metathesis (RCM) reactions was also evaluated to prepare benzolactam structures for evaluation as factor Xa inhibitors.

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Year:  2003        PMID: 14870853     DOI: 10.1023/b:modi.0000006826.91512.83

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  18 in total

1.  Microwave-assisted high-speed chemistry: a new technique in drug discovery.

Authors:  M Larhed; A Hallberg
Journal:  Drug Discov Today       Date:  2001-04-01       Impact factor: 7.851

Review 2.  High-speed combinatorial synthesis utilizing microwave irradiation.

Authors:  C Oliver Kappe
Journal:  Curr Opin Chem Biol       Date:  2002-06       Impact factor: 8.822

3.  Ligand-free palladium catalysis of the Suzuki reaction in water using microwave heating.

Authors:  Nicholas E Leadbeater; Maria Marco
Journal:  Org Lett       Date:  2002-08-22       Impact factor: 6.005

Review 4.  Microwave-accelerated homogeneous catalysis in organic chemistry.

Authors:  Mats Larhed; Christina Moberg; Anders Hallberg
Journal:  Acc Chem Res       Date:  2002-09       Impact factor: 22.384

5.  [The ganglion-blocking activities of some alkylamine derivatives of stilbene and of biphenyl].

Authors:  G CAVALLINI; P MANTEGAZZA; E MASSARANI; R TOMMASINI
Journal:  Farmaco Sci       Date:  1953

6.  Solution-phase synthesis of an aminomethyl-substituted biaryl library via sequential amine N-alkylation and Suzuki cross-coupling.

Authors:  M G Organ; E A Arvanitis; C E Dixon; D J Lavorato
Journal:  J Comb Chem       Date:  2001 Sep-Oct

7.  Discovery of 1-[3-(aminomethyl)phenyl]-N-3-fluoro-2'-(methylsulfonyl)-[1,1'-biphenyl]-4-yl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (DPC423), a highly potent, selective, and orally bioavailable inhibitor of blood coagulation factor Xa.

Authors:  D J Pinto; M J Orwat; S Wang; J M Fevig; M L Quan; E Amparo; J Cacciola; K A Rossi; R S Alexander; A M Smallwood; J M Luettgen; L Liang; B J Aungst; M R Wright; R M Knabb; P C Wong; R R Wexler; P Y Lam
Journal:  J Med Chem       Date:  2001-02-15       Impact factor: 7.446

8.  Rapid and amenable suzuki coupling reaction in water using microwave and conventional heating.

Authors:  Nicholas E Leadbeater; Maria Marco
Journal:  J Org Chem       Date:  2003-02-07       Impact factor: 4.354

9.  Selective effects of a 4-oxystilbene derivative on wild and mutant neuronal chick alpha7 nicotinic receptor.

Authors:  L Maggi; E Palma; F Eusebi; M Moretti; B Balestra; F Clementi; C Gotti
Journal:  Br J Pharmacol       Date:  1999-01       Impact factor: 8.739

10.  4-Oxystilbene compounds are selective ligands for neuronal nicotinic alphaBungarotoxin receptors.

Authors:  C Gotti; B Balestra; M Moretti; G E Rovati; L Maggi; G Rossoni; F Berti; L Villa; M Pallavicini; F Clementi
Journal:  Br J Pharmacol       Date:  1998-07       Impact factor: 8.739

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