LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives
Department羰基合成与选择氧化国家重点实验室
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)
2011
Source PublicationOrg. Biomol. Chem.
ISSN1477-0520
Volume9Pages:5948-5950
AbstractN-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.
Subject Area物理化学
Funding Organizationthe MOST (2010CB833200);the NSFC (20872054;20732002;21072086);program 111
Indexed BySCI
Language英语
Citation statistics
Cited Times:23[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/393
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorShe XG(厍学功)
Recommended Citation
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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