Literature DB >> 27436791

Construction of Cyclopenta[b]indol-1-ones by a Tandem Gold(I)-Catalyzed Rearrangement/Nazarov Reaction and Application to the Synthesis of Bruceolline H.

Dina Scarpi1, Martina Petrović1, Béla Fiser2, Enrique Gómez-Bengoa2, Ernesto G Occhiato1.   

Abstract

A tandem gold(I)-catalyzed rearrangement/Nazarov reaction of enynyl acetates which efficiently provides cyclopenta[b]indol-1-ones as useful precursors for the synthesis of natural and bioactive compounds is described. The synthetic potential of the methodology is demonstrated by the first total synthesis of bruceolline H.

Entities:  

Year:  2016        PMID: 27436791     DOI: 10.1021/acs.orglett.6b01990

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


  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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