Literature DB >> 10814473

An enantioconvergent route to (-)-shikimic acid via a palladium-mediated elimination reaction.

N Yoshida1, K Ogasawara.   

Abstract

[reaction--see text] (-)-Shikimic acid, the key intermediate in the shikimate pathway in plants and microorganisms, has been synthesized in an enantioconvergent manner from both enantiomeric starting materials by employing a palladium-mediated elimination reaction as the key step.

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Year:  2000        PMID： 10814473     DOI： 10.1021/ol005805q

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Enantioconvergent synthesis of (+)-aphanorphine via asymmetric Pd-catalyzed alkene carboamination.

Authors:  Duy N Mai; Brandon R Rosen; John P Wolfe
Journal:  Org Lett       Date:  2011-05-10       Impact factor: 6.005

Review 2.  Enantioconvergent catalysis.

Authors:  Justin T Mohr; Jared T Moore; Brian M Stoltz
Journal:  Beilstein J Org Chem       Date:  2016-09-16       Impact factor: 2.883

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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