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One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids

An efficient one-pot synthesis of novel β-amino acid derivatives containing a thiadiazole moiety was developed using a chiral squaramide cinchona alkaloid as organocatalyst. The reactions afforded chiral β-amino acid derivatives in moderate yields and with moderate to excellent enantioselectivities....

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Detalles Bibliográficos
Autores principales: Zhang, Kankan, Liang, Xueping, He, Ming, Wu, Jian, Zhang, Yuping, Xue, Wei, Jin, Linhong, Yang, Song, Hu, Deyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270396/
https://www.ncbi.nlm.nih.gov/pubmed/23702920
http://dx.doi.org/10.3390/molecules18066142
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author Zhang, Kankan
Liang, Xueping
He, Ming
Wu, Jian
Zhang, Yuping
Xue, Wei
Jin, Linhong
Yang, Song
Hu, Deyu
author_facet Zhang, Kankan
Liang, Xueping
He, Ming
Wu, Jian
Zhang, Yuping
Xue, Wei
Jin, Linhong
Yang, Song
Hu, Deyu
author_sort Zhang, Kankan
collection PubMed
description An efficient one-pot synthesis of novel β-amino acid derivatives containing a thiadiazole moiety was developed using a chiral squaramide cinchona alkaloid as organocatalyst. The reactions afforded chiral β-amino acid derivatives in moderate yields and with moderate to excellent enantioselectivities. The present study demonstrated for the first time the use of a Mannich reaction catalyzed by a chiral bifunctional organocatalyst for the one-pot synthesis of novel β-amino acid derivatives bearing a 1,3,4-thiadiazole moiety on nitrogen.
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spelling pubmed-62703962018-12-17 One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids Zhang, Kankan Liang, Xueping He, Ming Wu, Jian Zhang, Yuping Xue, Wei Jin, Linhong Yang, Song Hu, Deyu Molecules Article An efficient one-pot synthesis of novel β-amino acid derivatives containing a thiadiazole moiety was developed using a chiral squaramide cinchona alkaloid as organocatalyst. The reactions afforded chiral β-amino acid derivatives in moderate yields and with moderate to excellent enantioselectivities. The present study demonstrated for the first time the use of a Mannich reaction catalyzed by a chiral bifunctional organocatalyst for the one-pot synthesis of novel β-amino acid derivatives bearing a 1,3,4-thiadiazole moiety on nitrogen. MDPI 2013-05-23 /pmc/articles/PMC6270396/ /pubmed/23702920 http://dx.doi.org/10.3390/molecules18066142 Text en © 2013 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/3.0/).
spellingShingle Article
Zhang, Kankan
Liang, Xueping
He, Ming
Wu, Jian
Zhang, Yuping
Xue, Wei
Jin, Linhong
Yang, Song
Hu, Deyu
One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title_full One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title_fullStr One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title_full_unstemmed One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title_short One-Pot Synthesis of Novel Chiral β-Amino Acid Derivatives by Enantioselective Mannich Reactions Catalyzed by Squaramide Cinchona Alkaloids
title_sort one-pot synthesis of novel chiral β-amino acid derivatives by enantioselective mannich reactions catalyzed by squaramide cinchona alkaloids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270396/
https://www.ncbi.nlm.nih.gov/pubmed/23702920
http://dx.doi.org/10.3390/molecules18066142
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