Literature DB >> 15760226

Ionic liquid-immobilized quinuclidine-catalyzed Morita-Baylis-Hillman reactions.

Xueling Mi1, Sanzhong Luo, Jin-Pei Cheng.   

Abstract

[reaction: see text] The ionic liquid-bound quinuclidine catalyzed Baylis-Hillman reactions were investigated. The IL-supported catalyst showed equally good catalytic activity as compared with its nonimmobilized counterpart. The corresponding Baylis-Hillman adducts were obtained in moderate to high yields in all the cases tested. The IL-supported quinuclidine can be readily recovered and reused six times without significant loss of catalytic activity.

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Year:  2005        PMID: 15760226     DOI: 10.1021/jo048391d

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


  3 in total

1.  Reactions of nitroxides XIII: Synthesis of the Morita-Baylis-Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, and DABCO and quinuclidine as catalysts.

Authors:  Jerzy Zakrzewski
Journal:  Beilstein J Org Chem       Date:  2012-09-12       Impact factor: 2.883

2.  Synthesis, Structural Analysis, and Biological Activities of Some Imidazolium Salts.

Authors:  Gühergül Uluçam; Murat Turkyilmaz
Journal:  Bioinorg Chem Appl       Date:  2018-05-22       Impact factor: 7.778

3.  HFIP Mediates a Direct C-C Coupling between Michael Acceptors and Eschenmoser's salt.

Authors:  Miran Lemmerer; Margaux Riomet; Ricardo Meyrelles; Boris Maryasin; Leticia González; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-03       Impact factor: 16.823

  3 in total

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