Literature DB >> 28731697

Total Synthesis of Bruceolline I.

Dina Scarpi1, Cristina Faggi2, Ernesto G Occhiato1.   

Abstract

The first total synthesis of the natural product bruceolline I, isolated in small quantities from the ethanol extract of Brucea mollis stems, was achieved in 29% yield over nine steps and with high enantiomeric purity (>98%). The key step of the process is the tandem gold-catalyzed rearrangement/Nazarov reaction of a propargylic acetate derivative. This synthesis provides a sufficient amount of synthesized bruceolline I for further bioassays.

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Year:  2017        PMID: 28731697     DOI: 10.1021/acs.jnatprod.7b00311

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  2 in total

Review 1.  Recent metal-catalysed approaches for the synthesis of cyclopenta[b]indoles.

Authors:  Thavaraj Vivekanand; Bishnupada Satpathi; Siddheshwar K Bankar; S S V Ramasastry
Journal:  RSC Adv       Date:  2018-05-22       Impact factor: 4.036

2.  Pentannulation of N-heterocycles by a tandem gold-catalyzed [3,3]-rearrangement/Nazarov reaction of propargyl ester derivatives: a computational study on the crucial role of the nitrogen atom.

Authors:  Giovanna Zanella; Martina Petrović; Dina Scarpi; Ernesto G Occhiato; Enrique Gómez-Bengoa
Journal:  Beilstein J Org Chem       Date:  2020-12-15       Impact factor: 2.883

  2 in total

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