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Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives
A three-step procedure for the synthesis of multifunctionalized heterocycles from a pyroglutamic acid derivative, glycidyl components and anilines by nucleophilic substitution and cobalt catalysis is presented.
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151071/ https://www.ncbi.nlm.nih.gov/pubmed/17900352 http://dx.doi.org/10.1186/1860-5397-3-28 |
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author | Dyker, Gerald Thöne, Andreas Henkel, Gerald |
author_facet | Dyker, Gerald Thöne, Andreas Henkel, Gerald |
author_sort | Dyker, Gerald |
collection | PubMed |
description | A three-step procedure for the synthesis of multifunctionalized heterocycles from a pyroglutamic acid derivative, glycidyl components and anilines by nucleophilic substitution and cobalt catalysis is presented. |
format | Text |
id | pubmed-2151071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-21510712007-12-21 Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives Dyker, Gerald Thöne, Andreas Henkel, Gerald Beilstein J Org Chem Full Research Paper A three-step procedure for the synthesis of multifunctionalized heterocycles from a pyroglutamic acid derivative, glycidyl components and anilines by nucleophilic substitution and cobalt catalysis is presented. Beilstein-Institut 2007-09-27 /pmc/articles/PMC2151071/ /pubmed/17900352 http://dx.doi.org/10.1186/1860-5397-3-28 Text en Copyright © 2007, Dyker et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Dyker, Gerald Thöne, Andreas Henkel, Gerald Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title | Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title_full | Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title_fullStr | Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title_full_unstemmed | Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title_short | Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
title_sort | reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151071/ https://www.ncbi.nlm.nih.gov/pubmed/17900352 http://dx.doi.org/10.1186/1860-5397-3-28 |
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