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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.,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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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. |
format | Online Article Text |
id | pubmed-8359136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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