Literature DB >> 29750851

Chemoenzymatic Synthesis of Advanced Intermediates for Formal Total Syntheses of Tetrodotoxin.

Daler Baidilov1, Lukas Rycek1, John F Trant1, Jordan Froese1, Brennan Murphy1, Tomas Hudlicky1.   

Abstract

Advanced intermediates for the syntheses of tetrodotoxin reported by the groups of Fukuyama, Alonso, and Sato were prepared. Key steps include the toluene dioxygenase mediated dihydroxylation of either iodobenzene or benzyl acetate. The resulting diene diols were transformed into Fukuyama's intermediate in six steps, into Alonso's intermediate in nine steps, and into Sato's intermediate in ten steps.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  chemoenzymatic synthesis; formal synthesis; hydride shift; tetrodotoxin; total synthesis

Mesh:

Substances:

Year:  2018        PMID: 29750851     DOI: 10.1002/anie.201804602

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

Review 1.  Benefits of Unconventional Methods in the Total Synthesis of Natural Products.

Authors:  Tomas Hudlicky
Journal:  ACS Omega       Date:  2018-12-14
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.