Literature DB >> 14602020

Synthesis of the integrastatin nucleus using the Ramberg-Bäcklund reaction.

Jonathan S Foot1, Gerard M P Giblin, Richard J K Taylor.   

Abstract

[reaction: see text] The first synthesis of the tetracyclic nucleus of the Integrastatins, natural products that have been shown to selectively inhibit HIV-1 integrase, is reported. Key steps of this synthesis involve a novel cis-selective Ramberg-Bäcklund reaction and an unusual Lewis acid-promoted cyclization step.

Entities:  

Year:  2003        PMID: 14602020     DOI: 10.1021/ol035786v

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


  2 in total

1.  An amine template strategy to construct successive C-C bonds: synthesis of benzo[h]quinolines by a deaminative ring contraction cascade.

Authors:  Timothy Patrick McFadden; Chideraa Iheanyi Nwachukwu; Andrew George Roberts
Journal:  Org Biomol Chem       Date:  2022-02-16       Impact factor: 3.876

2.  Cyclization Reaction of 3,5-Diacetyl-2,6-dimethylpyridine with Salicylic Aldehyde and Its Derivatives: Quantum-Chemical Study and Molecular Docking.

Authors:  A L Stalinskaya; S Y Chikunov; I A Pustolaikina; I V Kulakov
Journal:  Russ J Gen Chem       Date:  2022-06-14       Impact factor: 0.779

  2 in total

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