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One-Pot Synthesis of α-Alkyl Styrene Derivatives

[Image: see text] There is a significant need to develop more rapid and efficient routes to styrene derivatives, since they are extensively used in polymer sciences. This manuscript reports a one-pot synthesis of an array of α-alkyl styrene derivatives from readily available natural products (i.e.,...

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Autores principales: Ojo, Olatunji S., Bugarin, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359136/
https://www.ncbi.nlm.nih.gov/pubmed/34396007
http://dx.doi.org/10.1021/acsomega.1c02801
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author Ojo, Olatunji S.
Bugarin, Alejandro
author_facet Ojo, Olatunji S.
Bugarin, Alejandro
author_sort Ojo, Olatunji S.
collection PubMed
description [Image: see text] There is a significant need to develop more rapid and efficient routes to styrene derivatives, since they are extensively used in polymer sciences. This manuscript reports a one-pot synthesis of an array of α-alkyl styrene derivatives from readily available natural products (i.e., estragole and safrole). This method is regioselective, producing a rearranged adduct, under transition metal-free conditions. This methodology has broad nucleophile scope, even tolerating sterically hindered nucleophiles; it is general for carbon, nitrogen, oxygen, and sulfur nucleophiles.
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spelling pubmed-83591362021-08-13 One-Pot Synthesis of α-Alkyl Styrene Derivatives Ojo, Olatunji S. Bugarin, Alejandro ACS Omega [Image: see text] There is a significant need to develop more rapid and efficient routes to styrene derivatives, since they are extensively used in polymer sciences. This manuscript reports a one-pot synthesis of an array of α-alkyl styrene derivatives from readily available natural products (i.e., estragole and safrole). This method is regioselective, producing a rearranged adduct, under transition metal-free conditions. This methodology has broad nucleophile scope, even tolerating sterically hindered nucleophiles; it is general for carbon, nitrogen, oxygen, and sulfur nucleophiles. American Chemical Society 2021-07-28 /pmc/articles/PMC8359136/ /pubmed/34396007 http://dx.doi.org/10.1021/acsomega.1c02801 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 Ojo, Olatunji S.
Bugarin, Alejandro
One-Pot Synthesis of α-Alkyl Styrene Derivatives
title One-Pot Synthesis of α-Alkyl Styrene Derivatives
title_full One-Pot Synthesis of α-Alkyl Styrene Derivatives
title_fullStr One-Pot Synthesis of α-Alkyl Styrene Derivatives
title_full_unstemmed One-Pot Synthesis of α-Alkyl Styrene Derivatives
title_short One-Pot Synthesis of α-Alkyl Styrene Derivatives
title_sort one-pot synthesis of α-alkyl styrene derivatives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359136/
https://www.ncbi.nlm.nih.gov/pubmed/34396007
http://dx.doi.org/10.1021/acsomega.1c02801
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