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Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin
A novel synthetic strategy for obtainment of (±)-3-deoxyradicinin (2) is reported. This synthetic methodology is more efficient than those previously reported in the literature and also shows higher versatility towards the introduction of different side-chains at both C-7 and C-2. The obtained compo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749313/ https://www.ncbi.nlm.nih.gov/pubmed/31484319 http://dx.doi.org/10.3390/molecules24173193 |
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author | Marsico, Giulia Ciccone, Maria Sabrina Masi, Marco Freda, Fabrizio Cristofaro, Massimo Evidente, Antonio Superchi, Stefano Scafato, Patrizia |
author_facet | Marsico, Giulia Ciccone, Maria Sabrina Masi, Marco Freda, Fabrizio Cristofaro, Massimo Evidente, Antonio Superchi, Stefano Scafato, Patrizia |
author_sort | Marsico, Giulia |
collection | PubMed |
description | A novel synthetic strategy for obtainment of (±)-3-deoxyradicinin (2) is reported. This synthetic methodology is more efficient than those previously reported in the literature and also shows higher versatility towards the introduction of different side-chains at both C-7 and C-2. The obtained compound (±)-2 shows phytotoxicity against the grass-weed buffelgrass comparable to that of the natural phytotoxin radicinin (1). Therefore, (±)-2 can constitute a more practical synthetic alternative to 1 as bioherbicide for buffelgrass control. |
format | Online Article Text |
id | pubmed-6749313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67493132019-09-27 Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin Marsico, Giulia Ciccone, Maria Sabrina Masi, Marco Freda, Fabrizio Cristofaro, Massimo Evidente, Antonio Superchi, Stefano Scafato, Patrizia Molecules Article A novel synthetic strategy for obtainment of (±)-3-deoxyradicinin (2) is reported. This synthetic methodology is more efficient than those previously reported in the literature and also shows higher versatility towards the introduction of different side-chains at both C-7 and C-2. The obtained compound (±)-2 shows phytotoxicity against the grass-weed buffelgrass comparable to that of the natural phytotoxin radicinin (1). Therefore, (±)-2 can constitute a more practical synthetic alternative to 1 as bioherbicide for buffelgrass control. MDPI 2019-09-03 /pmc/articles/PMC6749313/ /pubmed/31484319 http://dx.doi.org/10.3390/molecules24173193 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Marsico, Giulia Ciccone, Maria Sabrina Masi, Marco Freda, Fabrizio Cristofaro, Massimo Evidente, Antonio Superchi, Stefano Scafato, Patrizia Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title | Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title_full | Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title_fullStr | Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title_full_unstemmed | Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title_short | Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin |
title_sort | synthesis and herbicidal activity against buffelgrass (cenchrus ciliaris) of (±)-3-deoxyradicinin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749313/ https://www.ncbi.nlm.nih.gov/pubmed/31484319 http://dx.doi.org/10.3390/molecules24173193 |
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