Literature DB >> 15068079

Functionalised enones as starting materials for the construction of aziridine scaffolds.

Stefania Fioravanti1, Alberto Morreale, Lucio Pellacani, Paolo A Tardella.   

Abstract

alpha-Substituted beta-keto esters have been transformed by means of a straightforward procedure into aziridine-1,2-dicarboxylates, which have been efficiently converted into alkenyl aziridine-1,2-dicarboxylates through Wittig olefination reaction. The possibility of aziridine ring elaborations and the presence of an olefin function make these new molecules suitable scaffolds for further derivatisation into potential bioactive targets.

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Year:  2003        PMID: 15068079     DOI: 10.1023/b:modi.0000006757.23657.11

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  6 in total

Review 1.  Solution- and solid-phase strategies for the design, synthesis, and screening of libraries based on natural product templates: a comprehensive survey.

Authors:  D G Hall; S Manku; F Wang
Journal:  J Comb Chem       Date:  2001 Mar-Apr

2.  Methodologies for Generating Solution-Phase Combinatorial Libraries.

Authors:  Haoyun An; P. Dan Cook
Journal:  Chem Rev       Date:  2000-09-15       Impact factor: 60.622

3.  Click Chemistry: Diverse Chemical Function from a Few Good Reactions.

Authors:  Hartmuth C. Kolb; M. G. Finn; K. Barry Sharpless
Journal:  Angew Chem Int Ed Engl       Date:  2001-06-01       Impact factor: 15.336

4.  Synthesis and Aza-[2,3]-Wittig Rearrangements of Vinylaziridines: Scope and Limitations.

Authors:  Jens Åhman; Tomas Jarevång; Peter Somfai
Journal:  J Org Chem       Date:  1996-11-15       Impact factor: 4.354

5.  Diastereoselective aziridination of chiral alpha-carbonyl enoates.

Authors:  Stefania Fioravanti; Alberto Morreale; Lucio Pellacani; Paolo A Tardella
Journal:  J Org Chem       Date:  2002-07-12       Impact factor: 4.354

  6 in total

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