N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives
Qi J(齐静) ; Xie XG(谢新刚) ; He JM(何金梅) ; Zhang L(张玲) ; Ma DH(马东辉) ; She XG(厍学功)
刊名Org. Biomol. Chem.
2011
卷号9页码:5948-5950
ISSN号1477-0520
通讯作者厍学功
中文摘要N-Heterocyclic carbene was employed as an efficient organic catalyst to catalyze a cascade epoxide-opening and lactonization reaction. This organocatalytic process could transform various readily accessible c-epoxy-a,b-enals into dihydropyrone derivatives in good to excellent yields.
学科主题物理化学
收录类别SCI
资助信息the MOST (2010CB833200);the NSFC (20872054;20732002;21072086);program 111
语种英语
WOS记录号WOS:000293756800009
公开日期2012-09-20
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/393]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Qi J,Xie XG,He JM,et al. N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives[J]. Org. Biomol. Chem.,2011,9:5948-5950.
APA 齐静,谢新刚,何金梅,张玲,马东辉,&厍学功.(2011).N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives.Org. Biomol. Chem.,9,5948-5950.
MLA 齐静,et al."N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives".Org. Biomol. Chem. 9(2011):5948-5950.
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