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Acid-free aza diels-alder reaction of Danishefsky's diene with lmines
Alternative TitleDanishefsky 二烯与亚胺在无酸催化条件下的氮杂DA反应
Yuan Y(袁宇); Li X(李欣); Ding KL(丁奎岭)
2002
Source PublicationOrg. Lett.
ISSN1523-7060
Volume4Issue:19Pages:3309-3311
AbstractA highly efficient aza Diels-Alder reaction of Danishefsky's diene with imines was found to occur in methanol in the absence of any acids at room temperature to give corresponding 2-substituted dihydro-4-pyridone derivatives in high yields. This reaction can be also carried out in a three-componet one-pot reaction manner. The reaction was found to proceed through a Mannich-type condensation mechanism.
Subject Area金属有机化学
Department中国科学院上海有机化学研究所金属有机化学开放实验室
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Indexed BySCI
Language英语
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/17735
Collection金属有机化学国家重点实验室
Corresponding AuthorDing KL(丁奎岭)
Recommended Citation
GB/T 7714
Yuan Y,Li X,Ding KL. Acid-free aza diels-alder reaction of Danishefsky's diene with lmines[J]. Org. Lett.,2002,4(19):3309-3311.
APA 袁宇,李欣,&丁奎岭.(2002).Acid-free aza diels-alder reaction of Danishefsky's diene with lmines.Org. Lett.,4(19),3309-3311.
MLA 袁宇,et al."Acid-free aza diels-alder reaction of Danishefsky's diene with lmines".Org. Lett. 4.19(2002):3309-3311.
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