Literature DB >> 20866058

A synthesis of oseltamivir (Tamiflu) starting from D-mannitol.

Ji S Ko1, Ji E Keum, Soo Y Ko.   

Abstract

A synthesis of oseltamivir (Tamiflu) was achieved starting from D-mannitol. A unique feature of the synthetic route is that an acyclic precursor was constructed, which was then cyclized in an intramolecular aldol reaction to form the Tamiflu skeleton. Throughout the synthesis, well-established, highly efficient reactions were employed, and no protection/deprotection sequence was needed.

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Year:  2010        PMID: 20866058     DOI: 10.1021/jo101517g

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Synthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines.

Authors:  Melinda Nonn; Loránd Kiss; Reijo Sillanpää; Ferenc Fülöp
Journal:  Beilstein J Org Chem       Date:  2012-01-17       Impact factor: 2.883

2.  Treating a Global Health Crisis with a Dose of Synthetic Chemistry.

Authors:  Melissa A Hardy; Brandon A Wright; J Logan Bachman; Timothy B Boit; Hannah M S Haley; Rachel R Knapp; Robert F Lusi; Taku Okada; Veronica Tona; Neil K Garg; Richmond Sarpong
Journal:  ACS Cent Sci       Date:  2020-06-30       Impact factor: 14.553

Review 3.  The evolution of Tamiflu synthesis, 20 years on: Advent of enabling technologies the last piece of the puzzle?

Authors:  Cloudius R Sagandira; Francis M Mathe; Upenyu Guyo; Paul Watts
Journal:  Tetrahedron       Date:  2020-07-26       Impact factor: 2.457

  3 in total

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