Enantioselective synthesis of 1,2,4-triazolines catalyzed by a cinchona alkaloid-derived organocatalyst
出版年份 2013 全文链接
标题
Enantioselective synthesis of 1,2,4-triazolines catalyzed by a cinchona alkaloid-derived organocatalyst
作者
关键词
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出版物
CHEMICAL COMMUNICATIONS
Volume 49, Issue 94, Pages 11098
出版商
Royal Society of Chemistry (RSC)
发表日期
2013-10-10
DOI
10.1039/c3cc46757k
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Enantioselective synthesis of 1,2,4-triazolines by chiral iron(ii)-complex catalyzed cyclization of α-isocyano esters and azodicarboxylates
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- Cinchona Alkaloid Squaramide Catalyzed Enantioselective Hydrazination/Cyclization Cascade Reaction of α-Isocyanoacetates and Azodicarboxylates: Synthesis of Optically Active 1,2,4-Triazolines
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- Synthesis of 1,2,4-Triazolines and Triazoles Utilizing Oxazolones
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- Synthesis of 1,2,4-Triazolines: Base-Catalyzed Hydrazination/Cyclization Cascade of α-Isocyano Esters and Amides
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- Facile synthesis of 1,2,4-triazolines via PPh3-triggered reaction of azodicarboxylate with 2-azidoacrylates
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- Amide-based bifunctional organocatalysts in asymmetric reactions
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- Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts
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