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Highly Diastereoselective Synthesis of Spiropyrazolones
We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272153/ https://www.ncbi.nlm.nih.gov/pubmed/25985358 http://dx.doi.org/10.3390/molecules20058574 |
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author | Ceban, Victor Olomola, Temitope O. Meazza, Marta Rios, Ramon |
author_facet | Ceban, Victor Olomola, Temitope O. Meazza, Marta Rios, Ramon |
author_sort | Ceban, Victor |
collection | PubMed |
description | We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields. |
format | Online Article Text |
id | pubmed-6272153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62721532019-01-07 Highly Diastereoselective Synthesis of Spiropyrazolones Ceban, Victor Olomola, Temitope O. Meazza, Marta Rios, Ramon Molecules Communication We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields. MDPI 2015-05-13 /pmc/articles/PMC6272153/ /pubmed/25985358 http://dx.doi.org/10.3390/molecules20058574 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Ceban, Victor Olomola, Temitope O. Meazza, Marta Rios, Ramon Highly Diastereoselective Synthesis of Spiropyrazolones |
title | Highly Diastereoselective Synthesis of Spiropyrazolones |
title_full | Highly Diastereoselective Synthesis of Spiropyrazolones |
title_fullStr | Highly Diastereoselective Synthesis of Spiropyrazolones |
title_full_unstemmed | Highly Diastereoselective Synthesis of Spiropyrazolones |
title_short | Highly Diastereoselective Synthesis of Spiropyrazolones |
title_sort | highly diastereoselective synthesis of spiropyrazolones |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272153/ https://www.ncbi.nlm.nih.gov/pubmed/25985358 http://dx.doi.org/10.3390/molecules20058574 |
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