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Calcium(ii)-catalyzed enantioselective conjugate additions of amines
The direct enantioselective chiral calcium(ii)·phosphate complex (Ca[CPA](2))-catalyzed conjugate addition of unprotected alkyl amines to maleimides was developed. This mild catalytic system represents a significant advance towards the general convergent asymmetric amination of α,β-unsaturated elect...
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/PMC5887857/ https://www.ncbi.nlm.nih.gov/pubmed/29675209 http://dx.doi.org/10.1039/c7sc05205g |
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author | Uno, Brice E. Dicken, Rachel D. Redfern, Louis R. Stern, Charlotte M. Krzywicki, Greg G. Scheidt, Karl A. |
author_facet | Uno, Brice E. Dicken, Rachel D. Redfern, Louis R. Stern, Charlotte M. Krzywicki, Greg G. Scheidt, Karl A. |
author_sort | Uno, Brice E. |
collection | PubMed |
description | The direct enantioselective chiral calcium(ii)·phosphate complex (Ca[CPA](2))-catalyzed conjugate addition of unprotected alkyl amines to maleimides was developed. This mild catalytic system represents a significant advance towards the general convergent asymmetric amination of α,β-unsaturated electrophiles, providing medicinally relevant chiral aminosuccinimide products in high yields and enantioselectivities. Furthermore, the catalyst can be reused directly from a previously chromatographed reaction and still maintain both high yield and selectivity. |
format | Online Article Text |
id | pubmed-5887857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58878572018-04-19 Calcium(ii)-catalyzed enantioselective conjugate additions of amines Uno, Brice E. Dicken, Rachel D. Redfern, Louis R. Stern, Charlotte M. Krzywicki, Greg G. Scheidt, Karl A. Chem Sci Chemistry The direct enantioselective chiral calcium(ii)·phosphate complex (Ca[CPA](2))-catalyzed conjugate addition of unprotected alkyl amines to maleimides was developed. This mild catalytic system represents a significant advance towards the general convergent asymmetric amination of α,β-unsaturated electrophiles, providing medicinally relevant chiral aminosuccinimide products in high yields and enantioselectivities. Furthermore, the catalyst can be reused directly from a previously chromatographed reaction and still maintain both high yield and selectivity. Royal Society of Chemistry 2018-01-10 /pmc/articles/PMC5887857/ /pubmed/29675209 http://dx.doi.org/10.1039/c7sc05205g Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Uno, Brice E. Dicken, Rachel D. Redfern, Louis R. Stern, Charlotte M. Krzywicki, Greg G. Scheidt, Karl A. Calcium(ii)-catalyzed enantioselective conjugate additions of amines |
title | Calcium(ii)-catalyzed enantioselective conjugate additions of amines
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title_full | Calcium(ii)-catalyzed enantioselective conjugate additions of amines
|
title_fullStr | Calcium(ii)-catalyzed enantioselective conjugate additions of amines
|
title_full_unstemmed | Calcium(ii)-catalyzed enantioselective conjugate additions of amines
|
title_short | Calcium(ii)-catalyzed enantioselective conjugate additions of amines
|
title_sort | calcium(ii)-catalyzed enantioselective conjugate additions of amines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887857/ https://www.ncbi.nlm.nih.gov/pubmed/29675209 http://dx.doi.org/10.1039/c7sc05205g |
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