Literature DB >> 15281733

Unprecedented stereospecific synthesis of a novel tetracyclic ring system, a hybrid of tetrahydropyrrolo[2,3-b]indole and tetrahydroimidazo[1,2-a]indole, via a domino reaction upon a tryptophan-derived amino nitrile.

Juan A González-Vera1, M Teresa García-López, Rosario Herranz.   

Abstract

Compounds containing a novel tetracyclic ring system, a hybrid of tetrahydropyrrolo[2,3-b]indole and tetrahydroimidazo[1,2-a]indole, are synthesized via an acid-mediated stereospecific domino tautomerization of a tryptophan-derived alpha-amino nitrile. Characterization of these new compounds and preliminary studies on the reactivity of the tetracyclic heterocyclic system are reported. [reaction: see text]

Entities:  

Year:  2004        PMID: 15281733     DOI: 10.1021/ol049222i

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


  2 in total

1.  The Domino Way to Heterocycles.

Authors:  Albert Padwa; Scott K Bur
Journal:  Tetrahedron       Date:  2007-06-18       Impact factor: 2.457

2.  Tricyclic Imidazolidin-4-ones by Witkop Oxidation of Tetrahydro-β-carbolines.

Authors:  Derek A Leas; Yuxiang Dong; Jered C Garrison; Xiaofang Wang; Edward L Ezell; Douglas E Stack; Jonathan L Vennerstrom
Journal:  J Org Chem       Date:  2020-01-10       Impact factor: 4.354

  2 in total

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