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Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives
[Image: see text] Sp(3)-rich compounds are underrepresented in libraries for probe- and drug-discovery, despite their promise of extending the range of accessible molecular shapes beyond planar geometries. With this in mind, a collection of single-enantiomer bicyclic, fused cyclopentenones underpinn...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5171204/ https://www.ncbi.nlm.nih.gov/pubmed/27978655 http://dx.doi.org/10.1021/acs.orglett.6b03118 |
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author | Nelson, Shawn D. Wawer, Mathias J. Schreiber, Stuart L. |
author_facet | Nelson, Shawn D. Wawer, Mathias J. Schreiber, Stuart L. |
author_sort | Nelson, Shawn D. |
collection | PubMed |
description | [Image: see text] Sp(3)-rich compounds are underrepresented in libraries for probe- and drug-discovery, despite their promise of extending the range of accessible molecular shapes beyond planar geometries. With this in mind, a collection of single-enantiomer bicyclic, fused cyclopentenones underpinned by a complexity-generating Pauson–Khand cyclization was synthesized. A fingerprint of biological actions of these compounds was determined immediately after synthesis using real-time annotation−a process relying on multiplexed measurements of alterations in cell morphological features. |
format | Online Article Text |
id | pubmed-5171204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-51712042017-12-07 Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives Nelson, Shawn D. Wawer, Mathias J. Schreiber, Stuart L. Org Lett [Image: see text] Sp(3)-rich compounds are underrepresented in libraries for probe- and drug-discovery, despite their promise of extending the range of accessible molecular shapes beyond planar geometries. With this in mind, a collection of single-enantiomer bicyclic, fused cyclopentenones underpinned by a complexity-generating Pauson–Khand cyclization was synthesized. A fingerprint of biological actions of these compounds was determined immediately after synthesis using real-time annotation−a process relying on multiplexed measurements of alterations in cell morphological features. American Chemical Society 2016-12-07 2016-12-16 /pmc/articles/PMC5171204/ /pubmed/27978655 http://dx.doi.org/10.1021/acs.orglett.6b03118 Text en Copyright © 2016 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 | Nelson, Shawn D. Wawer, Mathias J. Schreiber, Stuart L. Divergent Synthesis and Real-Time Biological Annotation of Optically Active Tetrahydrocyclopenta[c]pyranone Derivatives |
title | Divergent Synthesis and Real-Time Biological Annotation
of Optically Active Tetrahydrocyclopenta[c]pyranone
Derivatives |
title_full | Divergent Synthesis and Real-Time Biological Annotation
of Optically Active Tetrahydrocyclopenta[c]pyranone
Derivatives |
title_fullStr | Divergent Synthesis and Real-Time Biological Annotation
of Optically Active Tetrahydrocyclopenta[c]pyranone
Derivatives |
title_full_unstemmed | Divergent Synthesis and Real-Time Biological Annotation
of Optically Active Tetrahydrocyclopenta[c]pyranone
Derivatives |
title_short | Divergent Synthesis and Real-Time Biological Annotation
of Optically Active Tetrahydrocyclopenta[c]pyranone
Derivatives |
title_sort | divergent synthesis and real-time biological annotation
of optically active tetrahydrocyclopenta[c]pyranone
derivatives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5171204/ https://www.ncbi.nlm.nih.gov/pubmed/27978655 http://dx.doi.org/10.1021/acs.orglett.6b03118 |
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