H-bonding directed one-step synthesis of novel macrocyclic peptides from epsilon-aminoquinolinecarboxylic acid
文献类型：期刊论文
| 作者 | Li, Fei1; Gan, Quan2,3; Xue, Lin2,3; Wang, Zhong-ming1; Jiang, Hua2 |
| 刊名 | TETRAHEDRON LETTERS
 |
| 出版日期 | 2009-05-20 |
| 卷号 | 50期号:20页码:2367-2369 |
| 关键词 | Macrocycles Oligopeptides One-step Synthesis Aggregation |
| ISSN号 | 0040-4039 |
| DOI | 10.1016/j.tetlet.2009.02.207 |
| 英文摘要 | Two macrocyclic peptides 1a and 1b were synthesized directly from epsilon-aminoquinoliiiecarboxylic acid 2a and 2b, respectively. The preorganization of the uncyclized intermediates mediated by hydrogen bonding assisted the cyclization. The structures of 1a and 1b were characterized by (1)H and (13)C NMR spectroscopy and MALDI-TOF MS analysis. Solid state structure of la was investigated by single crystal X-ray studies. Their aggregation behaviors in solution were studied by both variable concentration and temperature (1)H NMR experiments. (C) 2009 Elsevier Ltd. All rights reserved. |
| 语种 | 英语 |
| WOS记录号 | WOS:000265517700019 |
| 出版者 | PERGAMON-ELSEVIER SCIENCE LTD |
| 源URL | [http://ir.iccas.ac.cn/handle/121111/67501]  |
| 专题 | 中国科学院化学研究所 |
| 通讯作者 | Wang, Zhong-ming |
| 作者单位 | 1.Beijing Univ Chem Technol, Fac Sci, Dept Organ Chem, Beijing 100029, Peoples R China 2.Chinese Acad Sci, Inst Chem, CAS Key Lab Photochem, Beijing 100190, Peoples R China 3.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China |
| 推荐引用方式 GB/T 7714 | Li, Fei,Gan, Quan,Xue, Lin,et al. H-bonding directed one-step synthesis of novel macrocyclic peptides from epsilon-aminoquinolinecarboxylic acid[J]. TETRAHEDRON LETTERS,2009,50(20):2367-2369. |
| APA | Li, Fei,Gan, Quan,Xue, Lin,Wang, Zhong-ming,&Jiang, Hua.(2009).H-bonding directed one-step synthesis of novel macrocyclic peptides from epsilon-aminoquinolinecarboxylic acid.TETRAHEDRON LETTERS,50(20),2367-2369. |
| MLA | Li, Fei,et al."H-bonding directed one-step synthesis of novel macrocyclic peptides from epsilon-aminoquinolinecarboxylic acid".TETRAHEDRON LETTERS 50.20(2009):2367-2369. |
入库方式： OAI收割
来源：化学研究所
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