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Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil

[Image: see text] Macrocyclic lactones have redolent characteristics of muscones that originate from the rectal musk organs of the musk deer. These lactones are the primary raw material in the flavor and fragrance industry and are also found within the cyclic frameworks of various bioactive molecule...

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Autores principales: Rana, Rohit, Shreya, Upadhyay, Rahul, Maurya, Sushil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495847/
https://www.ncbi.nlm.nih.gov/pubmed/34632196
http://dx.doi.org/10.1021/acsomega.1c03319
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author Rana, Rohit
Shreya,
Upadhyay, Rahul
Maurya, Sushil K.
author_facet Rana, Rohit
Shreya,
Upadhyay, Rahul
Maurya, Sushil K.
author_sort Rana, Rohit
collection PubMed
description [Image: see text] Macrocyclic lactones have redolent characteristics of muscones that originate from the rectal musk organs of the musk deer. These lactones are the primary raw material in the flavor and fragrance industry and are also found within the cyclic frameworks of various bioactive molecules. Due to great demand, many efforts have been made for their synthesis; however, strategies generating a large number of macrocyclic analogues from renewable resources have not been fully realized and are urgently required. Here, we outline a sustainable, straightforward, and eco-friendly approach to synthesize high-valued macrocyclic lactones utilizing olive oil under greener reaction conditions. The outlined method allows us to turn biomass into valuable 12- to 29-membered lactones and dilactones.
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spelling pubmed-84958472021-10-08 Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil Rana, Rohit Shreya, Upadhyay, Rahul Maurya, Sushil K. ACS Omega [Image: see text] Macrocyclic lactones have redolent characteristics of muscones that originate from the rectal musk organs of the musk deer. These lactones are the primary raw material in the flavor and fragrance industry and are also found within the cyclic frameworks of various bioactive molecules. Due to great demand, many efforts have been made for their synthesis; however, strategies generating a large number of macrocyclic analogues from renewable resources have not been fully realized and are urgently required. Here, we outline a sustainable, straightforward, and eco-friendly approach to synthesize high-valued macrocyclic lactones utilizing olive oil under greener reaction conditions. The outlined method allows us to turn biomass into valuable 12- to 29-membered lactones and dilactones. American Chemical Society 2021-09-20 /pmc/articles/PMC8495847/ /pubmed/34632196 http://dx.doi.org/10.1021/acsomega.1c03319 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Rana, Rohit
Shreya,
Upadhyay, Rahul
Maurya, Sushil K.
Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title_full Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title_fullStr Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title_full_unstemmed Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title_short Synthesis of Macrocyclic Lactones and Dilactones Using Olive Oil
title_sort synthesis of macrocyclic lactones and dilactones using olive oil
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495847/
https://www.ncbi.nlm.nih.gov/pubmed/34632196
http://dx.doi.org/10.1021/acsomega.1c03319
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