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Atom-Economical and Metal-Free Synthesis of Multisubstituted Furans from Intramolecular Aziridine Ring Opening
[Image: see text] Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-dione through aziridine ring opening by the internal carbonyl oxygen with the assistance of BF(3)·OEt(2), followed by aromatization. This synthetic method is free from any metal and is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645301/ https://www.ncbi.nlm.nih.gov/pubmed/31457314 http://dx.doi.org/10.1021/acsomega.7b01542 |
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author | Yadav, Nagendra Nath Jeong, Hyeonsu Ha, Hyun-Joon |
author_facet | Yadav, Nagendra Nath Jeong, Hyeonsu Ha, Hyun-Joon |
author_sort | Yadav, Nagendra Nath |
collection | PubMed |
description | [Image: see text] Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-dione through aziridine ring opening by the internal carbonyl oxygen with the assistance of BF(3)·OEt(2), followed by aromatization. This synthetic method is free from any metal and is atom-economical with all of the atoms in the starting material retained in the final product. |
format | Online Article Text |
id | pubmed-6645301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66453012019-08-27 Atom-Economical and Metal-Free Synthesis of Multisubstituted Furans from Intramolecular Aziridine Ring Opening Yadav, Nagendra Nath Jeong, Hyeonsu Ha, Hyun-Joon ACS Omega [Image: see text] Multisubstituted furans were prepared from dialkyl 2-(aziridin-2-ylmethylene)malonate and/or 1,3-dione through aziridine ring opening by the internal carbonyl oxygen with the assistance of BF(3)·OEt(2), followed by aromatization. This synthetic method is free from any metal and is atom-economical with all of the atoms in the starting material retained in the final product. American Chemical Society 2017-11-01 /pmc/articles/PMC6645301/ /pubmed/31457314 http://dx.doi.org/10.1021/acsomega.7b01542 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Yadav, Nagendra Nath Jeong, Hyeonsu Ha, Hyun-Joon Atom-Economical and Metal-Free Synthesis of Multisubstituted Furans from Intramolecular Aziridine Ring Opening |
title | Atom-Economical and Metal-Free Synthesis of Multisubstituted
Furans from Intramolecular Aziridine Ring Opening |
title_full | Atom-Economical and Metal-Free Synthesis of Multisubstituted
Furans from Intramolecular Aziridine Ring Opening |
title_fullStr | Atom-Economical and Metal-Free Synthesis of Multisubstituted
Furans from Intramolecular Aziridine Ring Opening |
title_full_unstemmed | Atom-Economical and Metal-Free Synthesis of Multisubstituted
Furans from Intramolecular Aziridine Ring Opening |
title_short | Atom-Economical and Metal-Free Synthesis of Multisubstituted
Furans from Intramolecular Aziridine Ring Opening |
title_sort | atom-economical and metal-free synthesis of multisubstituted
furans from intramolecular aziridine ring opening |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645301/ https://www.ncbi.nlm.nih.gov/pubmed/31457314 http://dx.doi.org/10.1021/acsomega.7b01542 |
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