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 Publication | Org. Biomol. Chem. |
ISSN | 1477-0520 |
Volume | 9Pages:5948-5950 |
Abstract | 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. |
Subject Area | 物理化学 |
Funding Organization | the MOST (2010CB833200);the NSFC (20872054;20732002;21072086);program 111 |
Indexed By | SCI |
Language | 英语 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://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 Author | She 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. |
Files in This Item: | ||||||
File Name/Size | DocType | Version | Access | License | ||
61-Org. Biomol. Chem(159KB) | 开放获取 | License | View Application Full Text |
Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.
Edit Comment