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General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products
Protected L-homoDMDP en-8 and its C-6 epimer en-7 were prepared through two different pathways starting from the vinylpyrrolidine en-9. Based on the NMR and X-ray analysis, the stereochemistry of homoDMDP at C-6 was confirmed to be consistent with reported data. Compounds en-7 and en-8 are general i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269708/ https://www.ncbi.nlm.nih.gov/pubmed/23749160 http://dx.doi.org/10.3390/molecules18066723 |
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author | Huang, Mu-Hua Li, Yi-Xian Jia, Yue-Mei Yu, Chu-Yi |
author_facet | Huang, Mu-Hua Li, Yi-Xian Jia, Yue-Mei Yu, Chu-Yi |
author_sort | Huang, Mu-Hua |
collection | PubMed |
description | Protected L-homoDMDP en-8 and its C-6 epimer en-7 were prepared through two different pathways starting from the vinylpyrrolidine en-9. Based on the NMR and X-ray analysis, the stereochemistry of homoDMDP at C-6 was confirmed to be consistent with reported data. Compounds en-7 and en-8 are general intermediates for the synthesis of a series of 6-C-alkylated DMDP-related natural products, such as broussonetine G, homoDMDP-7-O-apioside, homoDMDP-7-O-β-D-xyloside and so on. |
format | Online Article Text |
id | pubmed-6269708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62697082018-12-17 General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products Huang, Mu-Hua Li, Yi-Xian Jia, Yue-Mei Yu, Chu-Yi Molecules Article Protected L-homoDMDP en-8 and its C-6 epimer en-7 were prepared through two different pathways starting from the vinylpyrrolidine en-9. Based on the NMR and X-ray analysis, the stereochemistry of homoDMDP at C-6 was confirmed to be consistent with reported data. Compounds en-7 and en-8 are general intermediates for the synthesis of a series of 6-C-alkylated DMDP-related natural products, such as broussonetine G, homoDMDP-7-O-apioside, homoDMDP-7-O-β-D-xyloside and so on. MDPI 2013-06-06 /pmc/articles/PMC6269708/ /pubmed/23749160 http://dx.doi.org/10.3390/molecules18066723 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Huang, Mu-Hua Li, Yi-Xian Jia, Yue-Mei Yu, Chu-Yi General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title | General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title_full | General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title_fullStr | General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title_full_unstemmed | General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title_short | General Intermediates for the Synthesis of 6-C-Alkylated DMDP-Related Natural Products |
title_sort | general intermediates for the synthesis of 6-c-alkylated dmdp-related natural products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269708/ https://www.ncbi.nlm.nih.gov/pubmed/23749160 http://dx.doi.org/10.3390/molecules18066723 |
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