Literature DB >> 21175219

Smiles cascades toward heterocyclic scaffolds.

Laurent El Kaim1, Laurence Grimaud, Xavier F Le Goff, Aurélie Schiltz.   

Abstract

Two different Smiles rearrangements can be combined to afford a multicomponent formation of isoquinolinones and isoindolinones from nitro methyl salicylate. After a Ugi-Smiles four-component coupling, the base-triggered cyclization of the resulting adduct is followed by a ring contraction via a Truce-Smiles rearrangement.

Entities:  

Year:  2010        PMID: 21175219     DOI: 10.1021/ol1028817

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


  3 in total

1.  Synthesis of novel isoquinolinone and 1,2-dihydroisoquinoline scaffolds via Ugi reaction and ring opening reaction of furans.

Authors:  Fei Ji; Wen-bin Yi; Mu Sun; Mei-fang Lv; Chun Cai
Journal:  Mol Divers       Date:  2013-03-20       Impact factor: 2.943

2.  Diarylamine Synthesis via Desulfinylative Smiles Rearrangement.

Authors:  Thomas Sephton; Jonathan M Large; Sam Butterworth; Michael F Greaney
Journal:  Org Lett       Date:  2022-01-30       Impact factor: 6.005

3.  Application of heterocyclic aldehydes as components in Ugi-Smiles couplings.

Authors:  Katelynn M Mason; Michael S Meyers; Abbie M Fox; Sarah B Luesse
Journal:  Beilstein J Org Chem       Date:  2016-09-15       Impact factor: 2.883

  3 in total

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