Literature DB >> 19219867

Synthesis of two bioactive natural products: FR252921 and pseudotrienic acid B.

Dominique Amans1, Véronique Bellosta, Janine Cossy.   

Abstract

Concise and highly convergent syntheses of the immunosuppressive agent FR252921 and the related antimicrobial natural product pseudotrienic acid B were achieved from a common intermediate by using optically active titanium complexes to control the configuration of the stereogenic centers, a highly stereo- and regioselective cross-metathesis to generate the triene moieties, and a Stille cross-coupling to install the dienic units.

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Year:  2009        PMID: 19219867     DOI: 10.1002/chem.200802649

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  An enantioselective synthesis of the C3-C21 segment of the macrolide immunosuppressive agent FR252921.

Authors:  Arun K Ghosh; Samuel Rodriguez
Journal:  Tetrahedron Lett       Date:  2016-05-18       Impact factor: 2.415

2.  A Domino 10-Step Total Synthesis of FR252921 and Its Analogues, Complex Macrocyclic Immunosuppressants.

Authors:  Yong Chen; Guilhem Coussanes; Caroline Souris; Paul Aillard; Dainis Kaldre; Kathrin Runggatscher; Stefan Kubicek; Giovanni Di Mauro; Boris Maryasin; Nuno Maulide
Journal:  J Am Chem Soc       Date:  2019-08-22       Impact factor: 16.383

Review 3.  Unconventional Macrocyclizations in Natural Product Synthesis.

Authors:  Iakovos Saridakis; Daniel Kaiser; Nuno Maulide
Journal:  ACS Cent Sci       Date:  2020-09-21       Impact factor: 14.553

  3 in total

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