Synthesis of Naphthalimide Derivatives by the Claisen Rearrangement and their Fluorescence Spectra
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چکیده
منابع مشابه
Propargyl Claisen rearrangement: allene synthesis and beyond.
The propargyl Claisen rearrangement is a known protocol to gain access to functionalized allenes through the [3,3]-sigmatropic transformation of propargyl vinyl ethers. The correct use of appropriate propargyl vinyl ethers as starting materials coupled with suitable reaction conditions can aid in the development of new domino methodologies in which the allenes are valuable intermediates in rout...
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A concise synthesis of forbesione (1) and desoxymorellin (3) is presented. Central to the strategy is a biomimetic Claisen/Diels-Alder/Claisen reaction cascade that proceeds in a regioselective manner and produces the desired scaffold exclusively. The observed regioselectivity and product distribution of the Claisen/Diels-Alder/Claisen reaction are attributed to the electronic effects of the xa...
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Reductive Claisen rearrangement of 1-allyloxy-8-methoxy-9, 10-anthraquinone followed by demethylation and reduction, and of 1,8-bisallyloxy-9,lO-anthraquinone followed by reduction provides regiospecific syntheses of 2-propyl- and 2,7-dipropyl anthralin
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the study reflected in this thesis aims at finding out relationships between critical thinking (ct), and the reading sections of tofel and ielts tests. the study tries to find any relationships between the ct ability of students and their performance on reading tests of tofel and academic ielts. however, no research has ever been conducted to investigate the relationship between ct and the read...
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ژورنال
عنوان ژورنال: Journal of Synthetic Organic Chemistry, Japan
سال: 1972
ISSN: 0037-9980,1883-6526
DOI: 10.5059/yukigoseikyokaishi.30.549