Literature DB >> 23526632

The aza-Morita-Baylis-Hillman reaction: a mechanistic and kinetic study.

Christoph Lindner1, Yinghao Liu, Konstantin Karaghiosoff, Boris Maryasin, Hendrik Zipse.   

Abstract

The aza-Morita-Baylis-Hillman (aza-MBH) reaction has been studied in a variety of solvents, a selection of imine substrates and with various combinations of PPh3 and para-nitrophenol as the catalyst system. The measured kinetic data indicates that the effects of solvent and protic co-catalyst are strongly interdependent. These results are most easily reconciled with a mechanistic model involving the reversible protonation of zwitterionic intermediates in the catalytic cycle, which is also supported by (31)P NMR spectroscopy and quantum chemical studies.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2013        PMID: 23526632     DOI: 10.1002/chem.201204006

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

Review 1.  Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines.

Authors:  Hélène Pellissier
Journal:  Beilstein J Org Chem       Date:  2018-06-06       Impact factor: 2.883

2.  Metal-Organic Frameworks Invert Molecular Reactivity: Lewis Acidic Phosphonium Zwitterions Catalyze the Aldol-Tishchenko Reaction.

Authors:  Gerald Bauer; Daniele Ongari; Xiaoying Xu; Davide Tiana; Berend Smit; Marco Ranocchiari
Journal:  J Am Chem Soc       Date:  2017-12-08       Impact factor: 15.419

  2 in total

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