期刊论文详细信息
| TETRAHEDRON LETTERS | 卷:53 |
| Divergent total synthesis of the natural antimalarial marinoquinolines A, B, C, E and unnatural analogues | |
| Article | |
| Schwalm, Cristiane Storck1  Correia, Carlos Roque D.1  | |
| [1] Univ Estadual Campinas, UNICAMP, Inst Quim, BR-13084917 Campinas, SP, Brazil | |
| 关键词: Marinoquinolines; Antimalarial; Heck-Matsuda reactions; Pictet-Spengler; | |
| DOI : 10.1016/j.tetlet.2012.06.115 | |
| 来源: Elsevier | |
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【 摘 要 】
A new synthetic route to marinoquinolines was developed, allowing the synthesis of several structurally related compounds from a common key intermediate. Four natural marinoquinolines (A, B. C and E) and nine unnatural new analogues were prepared by this strategy, which features a Heck-Matsuda reaction in pure water and the Pictet-Spengler reaction as key steps. (C) 2012 Elsevier Ltd. All rights reserved.
【 授权许可】
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【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_tetlet_2012_06_115.pdf | 939KB |
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