Literature DB >> 12182599

Microwave-accelerated O-alkylation of carboxylic acids with O-alkylisoureas.

Stefano Crosignani1, Peter D White, Bruno Linclau.   

Abstract

[reaction: see text] Microwave-assisted O-alkylations of several carboxylic acids have been performed with three different O-alkylisoureas. All reactions are significantly faster compared to conventionally heated reactions, while retaining high chemoselectivity. The combination of microwave technology with the use of the solid-supported isourea 3 enables the synthetic chemist to obtain the pure methyl esters starting from the corresponding acids in less than an hour.

Entities:  

Year:  2002        PMID: 12182599     DOI: 10.1021/ol0263705

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


  2 in total

1.  Ester Formation via Symbiotic Activation Utilizing Trichloroacetimidate Electrophiles.

Authors:  Nivedita S Mahajani; Rowan I L Meador; Tomas J Smith; Sarah E Canarelli; Arijit A Adhikari; Jigisha P Shah; Christopher M Russo; Daniel R Wallach; Kyle T Howard; Alexandra M Millimaci; John D Chisholm
Journal:  J Org Chem       Date:  2019-05-30       Impact factor: 4.354

2.  Microwaves, supported-reagents and parallel synthesis: isocyanide and ester synthesis.

Authors:  Stefano Crosignani; Delphine Launay; Bruno Linclau; Mark Bradley
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

  2 in total

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