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Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines
Well-defined unnatural dipeptide-alcohols based on a cis-2,5-disubstitued pyrrolidine backbone were synthesized from commercially available starting materials meso-diethyl-2,5-dibromoadipate, (S)-(−)-1-phenylethylamine, and phenylalaninol. The structures of these unnatural dipeptide-alcohols are sup...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272547/ https://www.ncbi.nlm.nih.gov/pubmed/25679051 http://dx.doi.org/10.3390/molecules20022922 |
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author | Jia, Yan-Yan Li, Xiao-Ye Wang, Ping-An Wen, Ai-Dong |
author_facet | Jia, Yan-Yan Li, Xiao-Ye Wang, Ping-An Wen, Ai-Dong |
author_sort | Jia, Yan-Yan |
collection | PubMed |
description | Well-defined unnatural dipeptide-alcohols based on a cis-2,5-disubstitued pyrrolidine backbone were synthesized from commercially available starting materials meso-diethyl-2,5-dibromoadipate, (S)-(−)-1-phenylethylamine, and phenylalaninol. The structures of these unnatural dipeptide-alcohols are supported by HRMS, (1)H- and (13)C-NMR spectroscopy. These unnatural dipeptide-alcohols can act as building blocks for peptidomimetics. |
format | Online Article Text |
id | pubmed-6272547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62725472018-12-13 Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines Jia, Yan-Yan Li, Xiao-Ye Wang, Ping-An Wen, Ai-Dong Molecules Article Well-defined unnatural dipeptide-alcohols based on a cis-2,5-disubstitued pyrrolidine backbone were synthesized from commercially available starting materials meso-diethyl-2,5-dibromoadipate, (S)-(−)-1-phenylethylamine, and phenylalaninol. The structures of these unnatural dipeptide-alcohols are supported by HRMS, (1)H- and (13)C-NMR spectroscopy. These unnatural dipeptide-alcohols can act as building blocks for peptidomimetics. MDPI 2015-02-11 /pmc/articles/PMC6272547/ /pubmed/25679051 http://dx.doi.org/10.3390/molecules20022922 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jia, Yan-Yan Li, Xiao-Ye Wang, Ping-An Wen, Ai-Dong Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title | Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title_full | Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title_fullStr | Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title_full_unstemmed | Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title_short | Facile Access to Unnatural Dipeptide-Alcohols Based on cis-2,5-Disubstituted Pyrrolidines |
title_sort | facile access to unnatural dipeptide-alcohols based on cis-2,5-disubstituted pyrrolidines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272547/ https://www.ncbi.nlm.nih.gov/pubmed/25679051 http://dx.doi.org/10.3390/molecules20022922 |
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