Literature DB >> 16119947

Organocatalytic ring expansion of beta-lactams to gamma-lactams through a novel N1-C4 bond cleavage. direct synthesis of enantiopure succinimide derivatives.

Benito Alcaide1, Pedro Almendros, Gema Cabrero, M Pilar Ruiz.   

Abstract

Tetrabutylammonium cyanide (20 mol %) catalyzes ring expansion of 4-(arylimino)methylazetidin-2-ones 2 to 5-aryliminopyrrolidin-2-ones 3 through a novel N1-C4 bond cleavage of the beta-lactam nucleus. New, efficient one-pot protocols to enantiopure succinimide derivatives 3 and 4 from beta-lactam aldehydes 1 have also been developed. [reaction: see text]

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Year:  2005        PMID: 16119947     DOI: 10.1021/ol051504a

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


  3 in total

1.  Advances in the chemistry of β-lactam and its medicinal applications.

Authors:  Anushree Kamath; Iwao Ojima
Journal:  Tetrahedron       Date:  2012-08-07       Impact factor: 2.457

2.  Radical-mediated dehydrative preparation of cyclic imides using (NH4)2S2O8-DMSO: application to the synthesis of vernakalant.

Authors:  Dnyaneshwar N Garad; Subhash D Tanpure; Santosh B Mhaske
Journal:  Beilstein J Org Chem       Date:  2015-06-12       Impact factor: 2.883

3.  Effects of chirality on the antifungal potency of methylated succinimides obtained by Aspergillus fumigatus biotransformations. comparison with racemic ones.

Authors:  Maximiliano Sortino; Agustina Postigo; Susana Zacchino
Journal:  Molecules       Date:  2013-05-15       Impact factor: 4.411

  3 in total

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