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A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
Medium-sized heterocycles have recently received significant attention because of their potential roles as modulators of protein–protein interactions, but their molecular diversity and synthetic availability are still inadequate to meet the demand. To address these issues, we developed a new diverge...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335630/ https://www.ncbi.nlm.nih.gov/pubmed/30746098 http://dx.doi.org/10.1039/c8sc04061c |
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author | Choi, Yoona Kim, Heejun Park, Seung Bum |
author_facet | Choi, Yoona Kim, Heejun Park, Seung Bum |
author_sort | Choi, Yoona |
collection | PubMed |
description | Medium-sized heterocycles have recently received significant attention because of their potential roles as modulators of protein–protein interactions, but their molecular diversity and synthetic availability are still inadequate to meet the demand. To address these issues, we developed a new divergent synthetic pathway for skeletally distinct pyrimidine-containing medium-sized azacycles. We introduced N-quaternized pyrimidine-containing polyheterocycles as novel key intermediates for diversity-generating reactions via selective bond cleavages or migrations and prepared 14 discrete core skeletons in an efficient manner. The skeletal diversity of the resulting molecular frameworks was confirmed by chemoinformatic analysis. |
format | Online Article Text |
id | pubmed-6335630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-63356302019-02-11 A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy Choi, Yoona Kim, Heejun Park, Seung Bum Chem Sci Chemistry Medium-sized heterocycles have recently received significant attention because of their potential roles as modulators of protein–protein interactions, but their molecular diversity and synthetic availability are still inadequate to meet the demand. To address these issues, we developed a new divergent synthetic pathway for skeletally distinct pyrimidine-containing medium-sized azacycles. We introduced N-quaternized pyrimidine-containing polyheterocycles as novel key intermediates for diversity-generating reactions via selective bond cleavages or migrations and prepared 14 discrete core skeletons in an efficient manner. The skeletal diversity of the resulting molecular frameworks was confirmed by chemoinformatic analysis. Royal Society of Chemistry 2018-10-18 /pmc/articles/PMC6335630/ /pubmed/30746098 http://dx.doi.org/10.1039/c8sc04061c Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Choi, Yoona Kim, Heejun Park, Seung Bum A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy |
title | A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
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title_full | A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
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title_fullStr | A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
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title_full_unstemmed | A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
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title_short | A divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an N-quaternizing strategy
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title_sort | divergent synthetic pathway for pyrimidine-embedded medium-sized azacycles through an n-quaternizing strategy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335630/ https://www.ncbi.nlm.nih.gov/pubmed/30746098 http://dx.doi.org/10.1039/c8sc04061c |
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