Literature DB >> 21732641

Regioselective ring opening and isomerization reactions of 3,4-epoxyesters catalyzed by boron trifluoride.

Javier Izquierdo1, Santiago Rodríguez, Florenci V González.   

Abstract

Efficient ring opening of 3,4-epoxyesters with alcohols to produce 4-alkoxy-3-hydroxyesters and their isomerization into 4-ketoesters using boron trifluoride as the catalyst are presented. Both transformations are simple and efficient methods for the synthesis of the above named synthetically useful compounds.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21732641     DOI: 10.1021/ol201378w

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


  1 in total

1.  Formal [3+2] Cycloaddition Reactions of Electron-Rich Aryl Epoxides with Alkenes under Lewis Acid Catalysis Affording Tetrasubstituted Tetrahydrofurans.

Authors:  Víctor E Macías-Villamizar; Luís Cuca-Suárez; Santiago Rodríguez; Florenci V González
Journal:  Molecules       Date:  2020-02-06       Impact factor: 4.411

  1 in total

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