Literature DB >> 26306463

A novel synthesis of isoeugenol, [ring-(U)-(14)C].

John E Immoos1.   

Abstract

A novel method for the preparation of isoeugenol, [ring-(U)-(14)C] is presented. Phenols and phenyl esters substituted in the para position with 1-hydroxyethyl or 1-hydroxypropyl acetate esters when treated with 1,8-diazabicyclo[5.4.0]undec-7-ene in dimethylformamide (DMF) eliminate the alkyl carboxylate function to give the unsaturated compound. The reaction fails with unsubstituted or ether substituted phenyl 1-hydroxyacetate esters.
Copyright © 2015 John Wiley & Sons, Ltd.

Entities:  

Keywords:  carbon-14; deacetylation; guaiacol; isoeugenol; quinone methide

Mesh:

Substances:

Year:  2015        PMID: 26306463     DOI: 10.1002/jlcr.3329

Source DB:  PubMed          Journal:  J Labelled Comp Radiopharm        ISSN: 0362-4803            Impact factor:   1.921


  1 in total

1.  First total synthesis of chromanone A, preparation of related compounds and evaluation of their antifungal activity against Candida albicans, a biofilm forming agent.

Authors:  Iván Cortés; Estefanía Cordisco; Teodoro S Kaufman; Maximiliano A Sortino; Laura A Svetaz; Andrea B J Bracca
Journal:  RSC Adv       Date:  2021-06-01       Impact factor: 4.036

  1 in total

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