Literature DB >> 24053467

Single-step Ugi multicomponent reaction for the synthesis of phosphopeptidomimetics.

Andrea F G Gargano1, Stefanie Buchinger, Michal Kohout, Wolfgang Lindner, Michael Lämmerhofer.   

Abstract

This article describes the design and optimization of an effective microwave-assisted multicomponent reaction to produce a novel class of phosphopeptidomimetic compounds. When using aminophosphonic acids (α, β, γ), aldehydes, and isocyanides as reactants and alcohols as solvents, these building blocks are merged to functionalized amido-aminophosphonate structures in a novel Ugi-type one-pot transformation reaction. A high level of structural diversity can be achieved with this synthetic approach, providing a platform for the production of functionalized building blocks for novel bioactive molecules. The general scope of this multicomponent synthetic protocol is explored by variation of reaction parameters together with an evaluation of a diverse set of reaction substrates. The applicability of this reaction has been demonstrated by the synthesis of 17 distinct compounds giving yields in the range of 20-92%.

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Year:  2013        PMID: 24053467     DOI: 10.1021/jo401372x

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  With unprotected amino acids to tetrazolo peptidomimetics.

Authors:  Rudrakshula Madhavachary; Qian Wang; Alexander Dömling
Journal:  Chem Commun (Camb)       Date:  2017-07-27       Impact factor: 6.222

2.  A universal isocyanide for diverse heterocycle syntheses.

Authors:  Pravin Patil; Kareem Khoury; Eberhardt Herdtweck; Alexander Dömling
Journal:  Org Lett       Date:  2014-10-29       Impact factor: 6.005

Review 3.  Phosphonopeptides containing free phosphonic groups: recent advances.

Authors:  Paweł Kafarski
Journal:  RSC Adv       Date:  2020-07-09       Impact factor: 4.036

  3 in total

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