| A trans diacyloxylation of indoles | |
| Department | OSSO国家重点实验室 |
| Liu Q(刘强)1; Zhao QY(赵庆勇)1; Liu J(刘劼)1; Wu P(巫攀)1; Yi H(易宏)1; Lei AW(雷爱文)1,2; Lei AW(雷爱文) | |
| 2012 | |
| Source Publication | Chemical Communications
 |
| ISSN | 1359-7345 |
| Volume | 48Issue:26Pages:3239-3241 |
| Abstract | A trans diacyloxylation of indoles is accomplished by employing PhI(OAc)2 as the oxidant. A broad range of functional groups are well tolerated. Both the electronic properties of the N-protecting groups of indoles and the acidity of the reaction media play important roles in the selectivity of indole acyloxylation reactions. |
| Subject Area | 物理化学与绿色催化 |
| DOI | 10.1039/c2cc17815j |
| Funding Organization | Program for Changjiang Scholars and Innovative Research Team in University (IRT1030);National Natural Science Foundation of China (20972118;20832003);financial support from Wuhan University |
| Indexed By | SCI |
| Language | 英语 |
| compositor | 第二作者单位 |
| Citation statistics | |
| Document Type | 期刊论文 |
| Identifier | http://ir.licp.cn/handle/362003/3805 |
| Collection | 羰基合成与选择氧化国家重点实验室（OSSO） |
| Corresponding Author | Lei AW(雷爱文) |
| Affiliation | 1.Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China 2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China |
| Recommended Citation GB/T 7714 | Liu Q,Zhao QY,Liu J,et al. A trans diacyloxylation of indoles[J]. Chemical Communications,2012,48(26):3239-3241. |
| APA | Liu Q.,Zhao QY.,Liu J.,Wu P.,Yi H.,...&雷爱文.(2012).A trans diacyloxylation of indoles.Chemical Communications,48(26),3239-3241. |
| MLA | Liu Q,et al."A trans diacyloxylation of indoles".Chemical Communications 48.26(2012):3239-3241. |
| Files in This Item: | ||||||
| File Name/Size | DocType | Version | Access | License | ||
| 24.Chem. Commun., 20（1468KB） | 期刊论文 | 作者接受稿 | 开放获取 | CC BY-NC-SA | View Application Full Text | |
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