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A carbohydrate approach for the formal total synthesis of (−)-aspergillide C
An enantioselective formal total synthesis of aspergillide C is accomplished using commercially available tri-O-acetyl-D-galactal employing a Ferrier-type C-glycosylation, utilizing a Trost hydrosilylation and protodesilylation as key reactions.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311580/ https://www.ncbi.nlm.nih.gov/pubmed/25670981 http://dx.doi.org/10.3762/bjoc.10.329 |
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author | Srihari, Pabbaraja Hari Krishna, Namballa Sridhar, Ydhyam Kamal, Ahmed |
author_facet | Srihari, Pabbaraja Hari Krishna, Namballa Sridhar, Ydhyam Kamal, Ahmed |
author_sort | Srihari, Pabbaraja |
collection | PubMed |
description | An enantioselective formal total synthesis of aspergillide C is accomplished using commercially available tri-O-acetyl-D-galactal employing a Ferrier-type C-glycosylation, utilizing a Trost hydrosilylation and protodesilylation as key reactions. |
format | Online Article Text |
id | pubmed-4311580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-43115802015-02-10 A carbohydrate approach for the formal total synthesis of (−)-aspergillide C Srihari, Pabbaraja Hari Krishna, Namballa Sridhar, Ydhyam Kamal, Ahmed Beilstein J Org Chem Letter An enantioselective formal total synthesis of aspergillide C is accomplished using commercially available tri-O-acetyl-D-galactal employing a Ferrier-type C-glycosylation, utilizing a Trost hydrosilylation and protodesilylation as key reactions. Beilstein-Institut 2014-12-23 /pmc/articles/PMC4311580/ /pubmed/25670981 http://dx.doi.org/10.3762/bjoc.10.329 Text en Copyright © 2014, Srihari 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 | Letter Srihari, Pabbaraja Hari Krishna, Namballa Sridhar, Ydhyam Kamal, Ahmed A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title | A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title_full | A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title_fullStr | A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title_full_unstemmed | A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title_short | A carbohydrate approach for the formal total synthesis of (−)-aspergillide C |
title_sort | carbohydrate approach for the formal total synthesis of (−)-aspergillide c |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311580/ https://www.ncbi.nlm.nih.gov/pubmed/25670981 http://dx.doi.org/10.3762/bjoc.10.329 |
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