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.

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