Literature DB >> 16737295

[AlCl3 + 2THF]: a new and efficient catalytic system for Diels-Alder cycloaddition of alpha,beta-unsaturated carbonyl compounds under solvent-free conditions.

Francesco Fringuelli1, Rugiada Girotti, Ferdinando Pizzo, Luigi Vaccaro.   

Abstract

[AlCl(3) + 2THF] is a new catalytic system for the Diels-Alder cycloaddition under SFC and air atmosphere. By using equimolar amounts of reactants, this catalyst prevents the polymerization of the diene and allows the corresponding adducts to be isolated with high regio- and stereocontrol and in excellent yields. [reaction: see text]

Entities:  

Year:  2006        PMID: 16737295     DOI: 10.1021/ol060569q

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


  3 in total

Review 1.  Sustainable Solvent-Free Diels-Alder Approaches in the Development of Constructive Heterocycles and Functionalized Materials: A Review.

Authors:  Aluru Rammohan; Alexey P Krinochkin; Albert F Khasanov; Dmitry S Kopchuk; Grigory V Zyryanov
Journal:  Top Curr Chem (Cham)       Date:  2022-08-11

Review 2.  Lewis Acidic Ionic Liquids.

Authors:  Lucy C Brown; James M Hogg; Małgorzata Swadźba-Kwaśny
Journal:  Top Curr Chem (Cham)       Date:  2017-08-21

3.  New Experimental Conditions for Diels-Alder and Friedel-Crafts Alquilation Reactions with Thiophene: A New Selenocyanate with Potent Activity against Cancer.

Authors:  Gorka Calvo-Martín; Daniel Plano; Carmen Sanmartín
Journal:  Molecules       Date:  2022-02-01       Impact factor: 4.411

  3 in total

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