Literature DB >> 15141083

Synthetic studies of roquefortine C: synthesis of isoroquefortine C and a heterocycle.

David J Richard1, Bruno Schiavi, Madeleine M Joullié.   

Abstract

The syntheses of isoroquefortine C and a related heterocycle were achieved by implementation of both intra- and intermolecular vinyl amidation reactions. These accomplishments represent a significant advance in the use of these strategies in the generation of complex molecules.

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Year:  2004        PMID: 15141083      PMCID: PMC514418          DOI: 10.1073/pnas.0401407101

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  12 in total

1.  Toxin-producing species of Penicillium and the development of mycotoxins in must and homemade wine.

Authors:  T Möller; K Akerstrand; T Massoud
Journal:  Nat Toxins       Date:  1997

2.  Penitrem A and Roquefortine Production by Penicillium commune.

Authors:  R E Wagener; N D Davis; U L Diener
Journal:  Appl Environ Microbiol       Date:  1980-04       Impact factor: 4.792

3.  Isolation of roquefortine C from feed grain.

Authors:  P Häggblom
Journal:  Appl Environ Microbiol       Date:  1990-09       Impact factor: 4.792

4.  Palladium-catalyzed stereocontrolled vinylation of azoles and phenothiazine.

Authors:  Artyom Y Lebedev; Vyatcheslav V Izmer; Denis N Kazyul'kin; Irina P Beletskaya; Alexander Z Voskoboynikov
Journal:  Org Lett       Date:  2002-02-21       Impact factor: 6.005

5.  Two classes of alkaloid mycotoxins produced by Penicillium crustosum thom isolated from contaminated beer.

Authors:  R J Cole; J W Dorner; R H Cox; L W Raymond
Journal:  J Agric Food Chem       Date:  1983 May-Jun       Impact factor: 5.279

6.  Acute toxicity studies on roquefortine and PR toxin, metabolites of Penicillium roqueforti, in the mouse.

Authors:  D L Arnold; P M Scott; P F McGuire; J Harwig; E A Nera
Journal:  Food Cosmet Toxicol       Date:  1978-08

7.  Total synthesis of isoroquefortine C.

Authors:  Bruno M Schiavi; David J Richard; Madeleine M Joullié
Journal:  J Org Chem       Date:  2002-02-08       Impact factor: 4.354

Review 8.  Mycotoxins.

Authors:  J W Bennett; M Klich
Journal:  Clin Microbiol Rev       Date:  2003-07       Impact factor: 26.132

9.  Copper-catalyzed coupling of amides and carbamates with vinyl halides.

Authors:  Lei Jiang; Gabriel E Job; Artis Klapars; Stephen L Buchwald
Journal:  Org Lett       Date:  2003-10-02       Impact factor: 6.005

10.  Coupling in the absence of tertiary amines.

Authors:  M Bodanszky; M A Bednarek; A Bodanszky
Journal:  Int J Pept Protein Res       Date:  1982-10
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  6 in total

1.  Enantioselective total syntheses of plectosphaeroic acids B and C.

Authors:  Salman Y Jabri; Larry E Overman
Journal:  J Org Chem       Date:  2013-08-27       Impact factor: 4.354

2.  Enantioselective total synthesis of plectosphaeroic acid B.

Authors:  Salman Y Jabri; Larry E Overman
Journal:  J Am Chem Soc       Date:  2013-03-06       Impact factor: 15.419

3.  Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution.

Authors:  Christopher D Grant; Michael J Krische
Journal:  Org Lett       Date:  2009-10-15       Impact factor: 6.005

4.  Synthesis of monoalkylidene diketopiperazines and application to the synthesis of barettin.

Authors:  Elizabeth W Kelley; Skylar G Norman; Jonathan R Scheerer
Journal:  Org Biomol Chem       Date:  2017-10-18       Impact factor: 3.876

5.  Synthesis of 5-Cyano-Tryptophan as a Two-Dimensional Infrared Spectroscopic Reporter of Structure.

Authors:  Farzaneh Chalyavi; Philip H Gilmartin; Andrew J Schmitz; Michael W Fennie; Matthew J Tucker
Journal:  Angew Chem Int Ed Engl       Date:  2018-05-29       Impact factor: 15.336

6.  Total Synthesis of the Proposed Structure of (-)-Novofumigatamide, Isomers Thereof, and Analogues. Part I.

Authors:  Patricia García-Domínguez; Paula Lorenzo; Rosana Álvarez; Angel R de Lera
Journal:  J Org Chem       Date:  2022-09-22       Impact factor: 4.198

  6 in total

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