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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...

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Autores principales: Uno, Brice E., Dicken, Rachel D., Redfern, Louis R., Stern, Charlotte M., Krzywicki, Greg G., Scheidt, Karl A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
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.
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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
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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