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Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy
[Image: see text] Intermolecular couplings of simple building blocks using catalytic, stereoselective cross-Mannich reactions followed by intramolecular functional group-pairing reactions of easily accessed variants of the Mannich products are explored as a route to skeletally diverse small molecule...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2661762/ https://www.ncbi.nlm.nih.gov/pubmed/19275223 http://dx.doi.org/10.1021/ol900173t |
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author | Uchida, Takuya Rodriquez, Manuela Schreiber, Stuart L. |
author_facet | Uchida, Takuya Rodriquez, Manuela Schreiber, Stuart L. |
author_sort | Uchida, Takuya |
collection | PubMed |
description | [Image: see text] Intermolecular couplings of simple building blocks using catalytic, stereoselective cross-Mannich reactions followed by intramolecular functional group-pairing reactions of easily accessed variants of the Mannich products are explored as a route to skeletally diverse small molecules. The synthetic pathway yields products having 12 different skeletons using only three steps and has the potential to enable substantial stereochemical diversification in the future. |
format | Text |
id | pubmed-2661762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-26617622009-03-27 Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy Uchida, Takuya Rodriquez, Manuela Schreiber, Stuart L. Org Lett [Image: see text] Intermolecular couplings of simple building blocks using catalytic, stereoselective cross-Mannich reactions followed by intramolecular functional group-pairing reactions of easily accessed variants of the Mannich products are explored as a route to skeletally diverse small molecules. The synthetic pathway yields products having 12 different skeletons using only three steps and has the potential to enable substantial stereochemical diversification in the future. American Chemical Society 2009-03-10 2009-04-02 /pmc/articles/PMC2661762/ /pubmed/19275223 http://dx.doi.org/10.1021/ol900173t Text en Copyright © 2009 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. 40.75 |
spellingShingle | Uchida, Takuya Rodriquez, Manuela Schreiber, Stuart L. Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title | Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title_full | Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title_fullStr | Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title_full_unstemmed | Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title_short | Skeletally Diverse Small Molecules Using a Build/Couple/Pair Strategy |
title_sort | skeletally diverse small molecules using a build/couple/pair strategy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2661762/ https://www.ncbi.nlm.nih.gov/pubmed/19275223 http://dx.doi.org/10.1021/ol900173t |
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