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Asymmetric Intramolecular Oxa-Michael Reactions to Tetrahydrofurans/2H-Pyrans Catalyzed by Primary-Secondary Diamines
Alternative Title伯/仲胺催化分子内氧杂迈克尔加成合成手性四氢呋喃/四氢吡喃
Lu YP(陆颖鹏); Zou G(邹刚); Zhao G(赵刚)
2013
Source PublicationACS Catal.
ISSN2155-5435
Volume3Issue:6Pages:1356-1359
AbstractThe asymmetric intramolecular oxa-Michael reactions of alpha,beta-unsaturated ketones have been achieved by using readily accessible primary-secondary diamines as the organocatalysts, giving the synthetically useful tetrahydrofurans/2H-pyrans in good yiel
Subject Area有机化学
Department华东理工大学 ; 中国科学院上海有机化学研究所, 天然产物有机合成化学重点实验室
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Indexed BySCI
Language英语
WOS IDWOS:000320298800031
Citation statistics
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/29259
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorZou G(邹刚); Zhao G(赵刚)
Recommended Citation
GB/T 7714
Lu YP,Zou G,Zhao G. Asymmetric Intramolecular Oxa-Michael Reactions to Tetrahydrofurans/2H-Pyrans Catalyzed by Primary-Secondary Diamines[J]. ACS Catal.,2013,3(6):1356-1359.
APA 陆颖鹏,邹刚,&赵刚.(2013).Asymmetric Intramolecular Oxa-Michael Reactions to Tetrahydrofurans/2H-Pyrans Catalyzed by Primary-Secondary Diamines.ACS Catal.,3(6),1356-1359.
MLA 陆颖鹏,et al."Asymmetric Intramolecular Oxa-Michael Reactions to Tetrahydrofurans/2H-Pyrans Catalyzed by Primary-Secondary Diamines".ACS Catal. 3.6(2013):1356-1359.
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