Cargando…

Synthesis of Isomers of Eugenol

In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation o...

Descripción completa

Detalles Bibliográficos
Autores principales: Brauer, Gerhard M., Morris, Richard Warren, Howe, Willard B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1963
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319455/
https://www.ncbi.nlm.nih.gov/pubmed/31580585
http://dx.doi.org/10.6028/jres.067A.026
_version_ 1782509384103886848
author Brauer, Gerhard M.
Morris, Richard Warren
Howe, Willard B.
author_facet Brauer, Gerhard M.
Morris, Richard Warren
Howe, Willard B.
author_sort Brauer, Gerhard M.
collection PubMed
description In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation of chavibetol from eugenol was achieved by gas chromatography.
format Online
Article
Text
id pubmed-5319455
institution National Center for Biotechnology Information
language English
publishDate 1963
publisher [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology
record_format MEDLINE/PubMed
spelling pubmed-53194552019-10-01 Synthesis of Isomers of Eugenol Brauer, Gerhard M. Morris, Richard Warren Howe, Willard B. J Res Natl Bur Stand A Phys Chem Article In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation of chavibetol from eugenol was achieved by gas chromatography. [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1963 1963-06-01 /pmc/articles/PMC5319455/ /pubmed/31580585 http://dx.doi.org/10.6028/jres.067A.026 Text en https://creativecommons.org/publicdomain/zero/1.0/ The Journal of Research of the National Bureau of Standards Section A is a publication of the U.S. Government. The papers are in the public domain and are not subject to copyright in the United States. Articles from J Res may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Article
Brauer, Gerhard M.
Morris, Richard Warren
Howe, Willard B.
Synthesis of Isomers of Eugenol
title Synthesis of Isomers of Eugenol
title_full Synthesis of Isomers of Eugenol
title_fullStr Synthesis of Isomers of Eugenol
title_full_unstemmed Synthesis of Isomers of Eugenol
title_short Synthesis of Isomers of Eugenol
title_sort synthesis of isomers of eugenol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319455/
https://www.ncbi.nlm.nih.gov/pubmed/31580585
http://dx.doi.org/10.6028/jres.067A.026
work_keys_str_mv AT brauergerhardm synthesisofisomersofeugenol
AT morrisrichardwarren synthesisofisomersofeugenol
AT howewillardb synthesisofisomersofeugenol