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Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection

Fragment‐based lead generation has proven to be an effective means of identifying high‐quality lead compounds for drug discovery programs. However, the fragment screening sets often used are principally comprised of sp(2)‐rich aromatic compounds, which limits the structural (and hence biological) di...

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Autores principales: Twigg, David G., Kondo, Noriyasu, Mitchell, Sophie L., Galloway, Warren R. J. D., Sore, Hannah F., Madin, Andrew, Spring, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091628/
https://www.ncbi.nlm.nih.gov/pubmed/27596095
http://dx.doi.org/10.1002/anie.201606496
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author Twigg, David G.
Kondo, Noriyasu
Mitchell, Sophie L.
Galloway, Warren R. J. D.
Sore, Hannah F.
Madin, Andrew
Spring, David R.
author_facet Twigg, David G.
Kondo, Noriyasu
Mitchell, Sophie L.
Galloway, Warren R. J. D.
Sore, Hannah F.
Madin, Andrew
Spring, David R.
author_sort Twigg, David G.
collection PubMed
description Fragment‐based lead generation has proven to be an effective means of identifying high‐quality lead compounds for drug discovery programs. However, the fragment screening sets often used are principally comprised of sp(2)‐rich aromatic compounds, which limits the structural (and hence biological) diversity of the library. Herein, we describe strategies for the synthesis of a series of partially saturated bicyclic heteroaromatic scaffolds with enhanced sp(3) character. Subsequent derivatization led to a fragment collection featuring regio‐ and stereo‐controlled introduction of substituents on the saturated ring system, often with formation of new stereocenters.
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spelling pubmed-50916282016-11-09 Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection Twigg, David G. Kondo, Noriyasu Mitchell, Sophie L. Galloway, Warren R. J. D. Sore, Hannah F. Madin, Andrew Spring, David R. Angew Chem Int Ed Engl Communications Fragment‐based lead generation has proven to be an effective means of identifying high‐quality lead compounds for drug discovery programs. However, the fragment screening sets often used are principally comprised of sp(2)‐rich aromatic compounds, which limits the structural (and hence biological) diversity of the library. Herein, we describe strategies for the synthesis of a series of partially saturated bicyclic heteroaromatic scaffolds with enhanced sp(3) character. Subsequent derivatization led to a fragment collection featuring regio‐ and stereo‐controlled introduction of substituents on the saturated ring system, often with formation of new stereocenters. John Wiley and Sons Inc. 2016-09-06 2016-09-26 /pmc/articles/PMC5091628/ /pubmed/27596095 http://dx.doi.org/10.1002/anie.201606496 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Twigg, David G.
Kondo, Noriyasu
Mitchell, Sophie L.
Galloway, Warren R. J. D.
Sore, Hannah F.
Madin, Andrew
Spring, David R.
Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title_full Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title_fullStr Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title_full_unstemmed Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title_short Partially Saturated Bicyclic Heteroaromatics as an sp(3)‐Enriched Fragment Collection
title_sort partially saturated bicyclic heteroaromatics as an sp(3)‐enriched fragment collection
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091628/
https://www.ncbi.nlm.nih.gov/pubmed/27596095
http://dx.doi.org/10.1002/anie.201606496
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