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Zr(Otf)4-catalyzed direct three-component Mannich-type reaction of carbamates: An efficient one-step synthesis of N-protected β-aryl-β-amino ketones
Department羰基合成与选择氧化国家重点实验室
Yang L(杨磊); Xu LW(徐利文); Sun W(孙伟); Xia CG(夏春谷)
2008
Source PublicationLetters in Organic Chemistry
ISSN1570-1786
Volume5Issue:1Pages:34-37
AbstractCarbamates were reacted in one pot with aromatic aldehyde and ketones at ambient temperature in the presence of catalytic amount of Zr(OTf)4 to furnish the corresponding N-protected b-amino-b-aryl ketones in good yields.
KeywordAza-michael Reaction Mannich Reaction Zirconium One Pot Carbamate Amino Ketone
Subject Area清洁催化与生物转化
Funding Organizationthe National Natural Science Founder of China (No. 20572114;20625308)
Indexed BySCI
Language英语
Funding Project清洁催化与生物转化研究组
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/1974
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorXu LW(徐利文); Xia CG(夏春谷)
Recommended Citation
GB/T 7714
Yang L,Xu LW,Sun W,et al. Zr(Otf)4-catalyzed direct three-component Mannich-type reaction of carbamates: An efficient one-step synthesis of N-protected β-aryl-β-amino ketones[J]. Letters in Organic Chemistry,2008,5(1):34-37.
APA 杨磊,徐利文,孙伟,&夏春谷.(2008).Zr(Otf)4-catalyzed direct three-component Mannich-type reaction of carbamates: An efficient one-step synthesis of N-protected β-aryl-β-amino ketones.Letters in Organic Chemistry,5(1),34-37.
MLA 杨磊,et al."Zr(Otf)4-catalyzed direct three-component Mannich-type reaction of carbamates: An efficient one-step synthesis of N-protected β-aryl-β-amino ketones".Letters in Organic Chemistry 5.1(2008):34-37.
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