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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...

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Autores principales: Nelson, Shawn D., Wawer, Mathias J., Schreiber, Stuart L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
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.
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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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