Literature DB >> 28180228

Dyotropic rearrangements in natural product total synthesis and biosynthesis.

Cedric L Hugelshofer1, Thomas Magauer2.   

Abstract

Covering: up to January 2017This highlight article presents some recent examples of dyotropic rearrangements, which were applied in natural product total synthesis or proposed to occur in biosyntheses. The implementation of dyotropic reactions in the preparation of complex natural products has resulted in the development of elegant synthetic routes, and thereby highlights the utility of these powerful, yet relatively underrepresented, transformations.

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Year:  2017        PMID: 28180228     DOI: 10.1039/c7np00005g

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  4 in total

1.  A Unifying Synthesis Approach to the C18-, C19-, and C20-Diterpenoid Alkaloids.

Authors:  Kevin G M Kou; Svitlana Kulyk; Christopher J Marth; Jack C Lee; Nicolle A Doering; Beryl X Li; Gary M Gallego; Terry P Lebold; Richmond Sarpong
Journal:  J Am Chem Soc       Date:  2017-09-20       Impact factor: 15.419

2.  Diterpene Biosynthesis in Catenulispora acidiphila: On the Mechanism of Catenul-14-en-6-ol Synthase.

Authors:  Geng Li; Yue-Wei Guo; Jeroen S Dickschat
Journal:  Angew Chem Int Ed Engl       Date:  2020-12-10       Impact factor: 15.336

3.  Sigmatropic [1,5] Carbon Shift of Transient C3 Ammonium Enolates.

Authors:  Garrit Wicker; Rundong Zhou; Roland Schoch; Jan Paradies
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-10       Impact factor: 16.823

4.  Synthesis of Hydrofluoroolefin-Based Iodonium Reagent via Dyotropic Rearrangement and Its Utilization in Fluoroalkylation.

Authors:  János T Csenki; Balázs L Tóth; Ferenc Béke; Bálint Varga; Péter P Fehér; András Stirling; Zsuzsanna Czégény; Attila Bényei; Zoltán Novák
Journal:  Angew Chem Int Ed Engl       Date:  2022-08-09       Impact factor: 16.823

  4 in total

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